Process for the stereochemical inversion of (2S,3S)-2-amino-3-phenyl-1,3-propanediols into their (2R,3R) enantiomers

ABSTRACT

Intermediates for transforming (2S,3S)-2-amino-3-phenyl-1,3-propanediols into their (2R,3R)-enantiomers are described. The final compounds are useful intermediates for the synthesis of antibiotics like chloramphenicol, Thiamphenicol and Florfenicol.

This is a divisional application of U.S. Ser. No. 07/992,747, filed Dec.18, 1992, now U.S. Pat. No. 5,284,966, which in turn is a continuationof U.S. Ser. No. 07/599,881, filed Oct. 19, 1990, now U.S. Pat. No.5,202,484.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention concerns a process for the conversion of(2S,3S)-2-amino-3-phenyl-1,3-propanediols into their corresponding (2R,3R)-enantiomers.

2. Discussion of the Background

Many 2-amino-3-phenyl-1,3-propanediols are useful as intermediates forthe synthesis of antibiotics like Chloramphenicol (Merck Index. X Ed.,No. 2035, page 289) and Thiamphenicol (Merck Index, X Ed., No. 9140,page 1332). Often, their synthesis is accompanied with discard productshaving a wrong configuration. Said compounds may be collected under thefollowing formula ##STR1## wherein: X=H, NO₂, CH₃ S, CH₃ SO or CH₃ SO₂.

The compounds of formula I having the (2R,3R) configuration are usefulfor the synthesis of the above cited antibiotics while the enantiomers I(2S,3S) are generally discard products of the industrial synthesis.

The compounds of formula I wherein X=NO₂ are known asthreo-(2R,3R)-micamine and (2S,3S)-micamine while those in which X=CH₃ Sas threo-(2R,3R)-thiomicamine and (2S,3S)-thiomicamine.

A further compound under development having antibiotic activity isFlorfenicol (European Patent No. 14437-Schering Co.) which has astructure analogous to that of Thiamphenicol wherein instead of theprimary hydroxy group there is a fluorine atom.

The synthesis of Florfenicol,(2S,3R)-3-(4-methylsulphonylphenyl)-3-hydroxy-2-dichloroacetamido-1-fluoro-propane,may be carried out starting from (2R,3R)-thiomicamine (see also Europeanpatent application No. 130,633-Zambon S.p.A.).

Some of the processes for the synthesis of Chloramphenicol orThiamphenicol comprise the preparation of a racemic mixture of theisomers threo (2R,3R)+(2S,3S) of micamine or of thiomicamine. Thedesired threo (2R,3R) isomer is then separated by a resolution processand is converted into the antibiotic compound by N-dichloroacetylationand, in the case of Thiamphenicol, also by oxidation of the CH₃ S groupinto CH₃ SO₂.

The isomer threo-(2S,3S), on the contrary, is a discard product of thesynthesis which must be eliminated thus increasing the cost of thedesired isomer.

Some processes have been studied which allow the racemization of the(2S,3S)-intermediate, i.e. to convert them into a 1:1 mixture of thethreo (2R,3R) and (2S,3S)-isomers [Tetrahedron Letters, 29, 5561, (1988)and references cited therein].

From these racemates the (2R,3R)-isomer must be separated and the(2S,3S)-isomer must be racemized again.

The process for racemization of aminodiols thus becomes cumbersome. So,it would be useful to have available a process of the synthesis ofChloramphenicol and Thiamphenicol, by transforming directly the abovereported intermediates (formula I) having (2S,3S)-configuration intotheir (2R,3R) enantiomers useful for the synthesis of the compoundshaving antibiotic activity.

However, to our knowledge, there has never been previously described aprocess allowing said double inversion.

SUMMARY OF THE INVENTION

We have now found and it is the object of the present invention, amulti-step process with a low cost and high total yields, which allowsone to convert the above reported intermediates having(2S,3S)-configuration into the corresponding compounds having(2R,3R)-configuration.

The process for the inversion of both the stereogenic centres, theobject of the invention, comprises the following steps which will bedescribed in detail in the following.

A) Protection of the amino group and of the hydroxy in position 3 of the(2S,3S)-3-phenyl-2-amino-1,3-propanediols of formula ##STR2## whereinX=H, NO₂, CH₃ S, CH₃ SO or CH₃ SO₂.

B) Oxidation of the CH₂ OH group to formyl or formyl derivative, carboxyor carboxy-derivative and epimerization of the carbon atom alpha to theoxidized group.

C) Restoring of the primary alcoholic function by reduction of theoxidized group.

D) Removal of the protective groups introduced in step A andepimerization of the benzylic centre in position 3.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

In view of the fact that the process of the invention has particularimportance when applied to the synthesis of Thiamphenicol and, as belowreported, of Florfenicol and because of the fact that both thesecompounds may be prepared from (2R,3R)-thiomicamine or fromintermediates of the process, the process will be illustrated givingparticular relevance to its application to the inversion of thesterogenic centres of (2S,3S)-thiomicamine or from intermediates of theprocess, the process will be illustrated giving particular relevance toits application to the inversion of the stereogenic centres of(2S,3S)-thiomicamine.

It has to be understood that, whenever not differently specified, whatwill be illustrated for thiomicamine stands also for the otherintermediates of formula I.

In the following description by the term lower alkyl or lower alkoxy wemean a C₁ -C₄ alkyl or C₁ -C₄ alkoxy, by the term carboxy derivative wemean an alkoxycarbonyl group wherein the alkoxy has 1-4 carbon atoms, anaminocarbonyl group or a mono or dialkylaminocarbonyl group whereinalkyl has 1-4 carbon atoms, by formyl derivative we mean acetals orhemiacetals or hydrates of the aldehyde group and oximes or hydrazonesthereof, by the term acyl we mean an acyl radical of a lower carboxylicacid having 1-5 carbon atoms optionally substituted by 1 or 2 halogenatoms, in particular dichloro-acetyl, or of a benzoic acid optionallysubstituted by chlorine or bromine atoms or by lower alkyl groups.

Step A

The protection of the hydroxy group in position 3 and of the nitrogenatom is carried out, by procedures per se known, by the introduction oftwo different protecting groups (III-A) as well as by thecontemporaneous protection of the hydroxy and nitrogen by formation ofan oxazolidine derivative (III-B).

Protection of type A: is carried out by transforming the hydroxy in 3into an ether or into an ester and by acylation of the NH₂ group. Boththe reactions are carried out by per se conventional methods. Thetransformation in ether is that presently preferred and can beconveniently carried out by heating thiomicamine in alcohol (e.g.methanol or ethanol) in the presence of an excess of mineral acid (e.g.sulphuric acid).

The reaction affords in practically quantitative yield the etherderivative of configuration 2S,3S (e.g.3-phenyl-3-ethoxy-2-amino-1-propanol).

The acylation of the nitrogen atom is carried out by using an acylatingagent selected from carbonic or carboxylic acid halides, anhydrides oresters according to conventional techniques for the preparation ofamides.

By an economic point of view it is preferred to use acetyl chloride oracetic anhydride thus obtaining the corresponding acetamide. It is clearto the man of the art how the hydroxy and the amino groups may beprotected by a variety of methods compatible with the functional groupsof the molecule and that this does not represent a meaningful variationof the object of the invention. For a compendium of the known methodsfor the protection of hydroxy and amino groups reference is made to T.W. Greene "Protective Groups in Organic Synthesis", J. Wiley andSon--New York, chapters 2 and 7 respectively.

The two above reported reactions afford the protected(2S,3S)-thiomicamine of formula ##STR3## wherein R₁ represents a loweralkyl or acyl and R₂ represents hydrogen, a lower alkyl, dichloromethyl,phenyl, alkoxy or benzyloxy group.

Preferably, in the compounds of formula III-A, R₁ represents methyl orethyl and R₂ methyl.

By operating according to a completely analogous procedure, the analogsof the compounds of formula III-A derived from micamine or from theother intermediates of formula I may be prepared.

Protection of type B: it consists in preparing a derivative ofN-acyl-1,3-oxazolidine by a heterocyclic ring closure between thenitrogen and the hydroxy in position 3.

The oxazolidine is preferably prepared by first protecting the primaryhydroxy group as ester and the nitrogen as amide by conventionaltechniques.

Preferably, the acylating agent of the hydroxy (ester) and the nitrogen(amide) will be the same.

The reaction is carried out by reacting thiomicamine with an excess ofacylating agent (chloride, anhydride or ester of a carboxylic orcarbonic acid) to obtain by first a diester in which both the hydroxygroups of the molecule have been esterified. By basic catalysis thediester is transformed to the desired product of formula ##STR4##wherein the R₂ S, equal to or different from each other, have the samemeanings above reported.

The preparation of the compounds of formula IV-A has already beendescribed in Italian patent No. 1,186,716 (Zambon S.p.A) which concernsa process for the racemization of 2S,3S-threo-thiomicamine. Foreconomical reasons it is preferred to use as acylating agent an aceticderivative thus obtaining the compound IV-A wherein both the R₂ aremethyl.

In a practical embodiment the reaction is carried out in a single stepby reacting (2S,3S)-thiomicamine with 2 moles of acetyl chloride and 2moles of a non-nucleophilic organic base (e.g. Et₃ N) in an inertdiluent such as a chloroorganic aliphatic or aromatic solvent (e.g.methylene chloride, 1,2-dichloroethane, dichlorobenzene).

Alternatively, it is possible to prepare the N-acyl-derivative ofthiomicamine by reaction with an acyl chloride or chloroformiate andthen to esterify the primary hydroxy by conventional methods. Thethiomicamine protected both as ester on the primary hydroxy and as amideon the NH₂ is then transformed in an oxazolidine derivative of formula##STR5## wherein R₂ has the above reported meanings, R₃ and R₄ equal toor different from each other, represent hydrogen atoms, lower alkyls,phenyls, lower alkoxy or R₃ and R₄ together are an oxygen or sulphuratom or a tetra or pentamethylene chain.

The preparation of some of the compounds of formula III-B has beendescribed in European patent application No. 130,633 (Zambon S.p.A.)which concerns a process for the preparation of Florfenicol.

The preparation of the compounds of formula III-B from protectedthiomicamine comprises the condensation with an aldehyde or an acetalthereof (to obtain the compounds of formula III-b wherein R₃ =R₄ =H orR₃ =H and R₄ =alkyl or aryl) or with a ketone or a ketal thereof (for R₃and R₄ =alkyl or R₃ and R₄ together=tetra or pentamethylene chain), orwith an orthoformate (for R₃ =H and R₄ =alkoxy), with a chloroformate, adialkylcarbonate, a thiocarbonate (for R₃ and R₄ together=oxygen orsulphur atom).

Specific examples of compounds suitable for being condensed with theprotected thiomicamine to afford the oxazolidine are the following:formaldehyde, acetaldehyde, propionaldehyde, benzaldehyde and theiracetals, acetone, diethylketone, methyl-ethylketone, acetophenone,cyclopentanone, cyclohexanone and their ketals, trimethylorthoformate,triethylorthoformate, alkyl chloroformate, diethylcarbonate anddiethylthiocarbonate.

In order to avoid the introduction in the molecule of a new asymmetriccenter, it is preferred to prepare an oxazolidine wherein R₃ =R₄.Accordingly, formaldehyde and symmetrical ketones like acetone,diethylketone, cyclopentanone and cyclohexanone or their ketals arepreferred.

For economy reasons it is preferred to use formaldehyde, acetone or itsdimethylketal (2,2-dimethoxy-propane).

The condensation reaction is carried out in the presence of a catalyticamount of an acid, e.g. a sulphonic acid or sulphuric acid by avoiding,however, an excess of acid in the mixture, at a temperature comprisedbetween room temperature and 100° C., in an inert solvent.

The reaction affords the oxazolidine wherein the CH₂ OH group isprotected as ester according to the protection previously introduced onthe thiomicamine.

The oxazolidine of formula III-B is obtained by deprotecting saidhydroxy by treatment with an alkaline base in an alcoholic solventoptionally in the presence of water.

Alternatively, the preparation of oxazolidine III-B may be carried outby treating directly thiomicamine with an agent which can afford theoxazolidine, as cited above, which may also act as solvent (e.g. byusing acetone both as reactant and solvent) under azeotropicdistillation of the water formed in the reaction (e.g. in the presencealso of toluene).

Thereby, the oxazolidine of formula ##STR6## wherein R₃ and R₄ have theabove reported meanings, is obtained.

The N-acylation of compound IV-B by an acyl halide or ester in thepresence of a base or by an anhydride (e.g. acetic anhydride) providesthe oxazolidine III-B.

Also in this case, for the same reasons above reported, it is preferredthat R₃ and R₄ be equal to each other, e.g. R₃ =R₄ =CH₃. From the abovereported reactions, thiomicamine protected on both the hydroxy inposition 3 and the nitrogen in the form of an open chain (III-A) orcyclic (III-B) derivative, is thus obtained. For convenience, we collectunder a single formula (formula III) the two above described kinds ofprotection ##STR7## wherein R₂ has the above reported meanings, R₅represents a lower alkyl or acyl and R₆ a hydrogen atom or R₅ and R₆together are the group C(R₃)(R₄)- wherein R₃ and R₄ have the abovereported meanings.

By operating in an analogous way, the compounds of formula III derivedfrom micamine and from the other intermediates of formula I can beprepared.

Step B

It comprises the oxidation of the CH₂ OH group of the compounds offormula III and the epimerization of the carbon atom in alpha to theoxidized group.

The two steps have been collected in a single step because, depending onthe reaction conditions of the oxidation step, it is possible to have acontemporaneous epimerization.

Thus, the CH₂ OH group of compounds III is oxidized to formyl, carboxyor carboxy derivative like, preferably, methoxycarbonyl orethoxycarbonyl.

The oxidation reaction is preferably carried out by using reactants thatdo not oxidize the CH₃ S group present on the aromatic ring. For thispurpose, reference is made to J. March, "Advanced Organic Chemistry",3rd Edition, J. Wiley & Son--New York, for a compendium of the methodsfor oxidation of a primary alcohol to aldehyde or carboxy derivatives,and to the following papers:

A. J. Mancuso, D. Swern, Synthesis, 165, (1981)

D. F. Taber et al., J. Org. Chem., 52, 5621, (1987)

J. C. Collins, Tetrahedron Lett., 3363, (1968)

T. Miyazawa et al., J. Org. Chem., 50, 1332, (1985)

D. H. Hunter et al., J. Org. Chem., 53, 1278, (1988)

P. L. Anelli et al., J. Org. Chem., 52, 2559, (1987)

V. Franzen, Organic Synthesis Coll., vol. V, 872

S. Mukaiyama et al., Bull. Chem. Soc. Japan, 54, 2221, (1981) orreferences cited therein.

The Oppenhauer or the Swern-Moffat oxidations are useful for the purposeeven if any oxidant able to afford the desired chemoselectivity may beequally useful.

The experiments carried out according to the Swern conditions(dimethylsulphoxide, oxalyl chloride followed by triethylamine at lowtemperature) gave satisfactory results.

Alternatively, chlorine and dimethylsulphide or P₂ O₅ anddimethylsulphoxide and Et₃ N, or CrO₃ and pyridine or chlorine andpyridine, trichlorocyanuric acid and pyridine, N-chloroamides anddimethylsulphide or methyl-phenylsulphide, a benzenesulphonic acidchloride with dimethylsulphoxide and triethylamine, were used asreactants and afforded analogous results.

The oxidation of the hydroxymethyl group of compound III to carboxy oralkoxycarbonyl is carried out by known procedures too. Thereby areobtained the compounds of formula ##STR8## wherein R₂, R₅ and R₆ havethe above reported meanings and R₇ represents a hydrogen atom, hydroxy,alkoxy, preferably methoxy or ethoxy.

From the compound of formula V wherein R₇ =H (COR₇ =formyl) it ispossible to prepare the carbonyl derivatives like oximes, hydrazones,acetals, hemiacetals or hydrates, these latters may be prepared alsoduring the oxidation phase.

The preparation of the amides of the compounds of formula V (R₇ =amino,mono o dialkylamino) is carried out by known methods starting from thecompounds of formula I wherein R₇ =hydroxy or alkoxy.

Even if generally it is not necessary, the aim for transforming theformyl in a carbonyl derivative or the carboxy in amide is that ofmodifying the solubility in the different solvents in order to makeeasier the separation of the products.

The carbonyl derivatives may be then retransformed into formyl ordirectly reduced to hydroxymethyl according to the subsequent step.Preferably, the preparation of the compounds of formula V wherein R₇ isdifferent from hydrogen will be carried out by first preparing byoxidation the compounds wherein R₇ is alkoxy and from these, whendesired, the compounds wherein R₇ is hydroxy, amino, mono ordialkylamino.

The preferred compounds of formula V are those in which R₇ is a hydrogenatom and they are a further object of the present invention.

We recall that, according to nomenclature conventions, the replacementof the CH₂ OH group by a CO-R₇ group modifies the denomination of theconfiguration of the carbon atom in position 2 (from S to R) but thisdoes not mean that its initial absolute configuration is changed.

The presence of the formyl, alkoxycarbonyl or of the other above citedgroups in the compounds V allows the epimerization of the alpha carbonboth under acidic and basic conditions.

Therefore, this allows to obtain a mixture of compounds V havingconfiguration 2R,3S and 2S,3S. This latter one is the desired compoundin which the center in position 2 has inverted its configuration. Wehave surprisingly found that when the epimerization is carried out byusing non-nucleophilic bases such as tertiary amines [in particulartriethylamine; 1,5,7-triazacicyclo-[4,4,0]-dec-5-ene;1,8-diazabicyclo-[5,9,0]-undec-7-ene; or still, more preferably,diazabicyclooctane (DABCO)] preferably in a non-protic medium, anequilibrium mixture of compounds V (2R,3S) and (2S,3S) is obtained fromwhich, optionally by seeding V (2S,3S), the desired compoundprecipitates and contemporaneously the mixture of compounds V insolution re-equilibrates.

Thereby, the desired compound V (2S,3S) with high diastereomeric purityand in up to 90% yield is obtained.

This is a quite rare reaction, called "second order asymmetrictransformation", which to our knowledge finds few precedents incarbohydrate chemistry.

The same reaction may also be carried out with analogous results byoperating in the absence of solvents. In view of the high yield in V(2S,3S) the reaction crude may be used for the subsequent reactionwithout isolating the product, provided that the epimerization catalyst(acid or base) is eliminated or neutralized.

Obviously, as an alternative, it is possible to separate the oxidizedproduct also not under equilibrating conditions (e.g. by transformingthe formyl into a carbonyl derivative which modifies the solubility inthe reaction medium).

As above mentioned, the reaction conditions for the oxidation of thehydroxymethyl group in compounds III may afford a more or less advanceddegree of epimerization. In such case, e.g. by terminating the Swernoxidation with triethylamine, the subsequent treatment for withdrawingthe isomer V (2S,3S) from the equilibrium will be carried out.

By operating in an analogous way it is possible to prepare the analogsof compound V (2S,3S) derived from micamine or from the otherintermediates of formula I.

Obviously, in this case, the problem of undesired oxidations isdecreased thus broadening the choice of the oxidants and allowing aneasier synthesis of the compounds in which the CH₂ OH group is oxidized.

Step C

It consists in the reduction of the CO-R₇ group of compound V (2S,3S) tohydroxymethyl in order to obtain a compound of formula ##STR9## whereinR₂, R₅ and R₆ have the above reported meanings. We further recall thatthe change in the configuration of the carbon atom in 2 (from 2S incompound V to 2R in compound VI) is due only to nomenclature conventionsand does not correspond to an inversion of configuration.

The reduction of the CO-R₇ group to hydroxymethyl must be carried outunder conditions which do not result in an epimerization and which donot reduce other functional groups.

In particular, strongly acidic and basic conditions must be avoided. Itis thus necessary to use a substantially neutral reducing agent and/orto operate in the presence of a buffer.

A reducing agent suitable for industrial use is sodium borohydride inalcohol. In view of the fact that the industrial product might containsodium hydroxyde, it is preferred to use also a buffer, a calcium salt(e.g. CaCl₂) or a weak acid.

However, we have observed that when in compound V [(2S,3S)+(2R,3S)] R₇is hydrogen and the reduction is carried out in alcohol without addedbuffer, the reaction of the selected stereoisomer [V, (2S,3S)] to affordthe desired stereoisomer [VI, (2R,3S)] is faster thus allowing andincrease in its diastereomeric purity. This fact is meaningful inparticular when the compounds V and VI are oxazolidines.

For a compendium of the known reduction methods reference is made to J.March above cited.

By operating according to these conditions the reduction is highlyselective and affords compound VI (2R,3S) in high yield and purity. Byoperating an analogous way the analogs of compound VI (2R,3S) derivedfrom micamine or from the other intermediates of formula I are prepared.

Step D

It consists in the deprotection of the hydroxy in 3 and of the amino in2 and in the epimerization of the benzylic carbon atom in 3. Thereactions have been collected under a single step because they may becarried out in the same reaction vessel, because the deprotection, whencarried out according to the below reported experimental conditions,already affords the epimerized product and also because theepimerization reaction may precede that of deprotection. Step D may beconveniently carried out by heating, at a temperature comprised between20° and 100° C., a suspension of compound VI (2R,3S) in water containing1-3 equivalents of a strong acid for each mole of compound VI.

Suitable acids are hydrochloric, hydrobromic, sulphuric,methanesulphonic and p.toluenesulphonic acid.

We have surprisingly found that under these conditions the2R,3S-thiomicamine is in equilibrium with the desired 2R,3R-enantiomer.Further studies allowed to find out other experimental conditions, belowillustrated, which allow this quite useful equilibrium to occur.

In a short time compound VI (2R,3S) is hydrolized to N-acyl-aminodioland in a longer time the epimerization of the carbon in position 3occurs. This important observation allows to realize also an alternativeto the process which will be illustrated in the following.

At the equilibrium the ratio between thiomicamine 2R,3S and 2R,3R isabout 30:70.

By cooling the equilibrium solution the (2R,3R)-thiomicamine, i.e. theproduct of double inversion with respect to the starting product,precipitates in the form of a salt with the acid present. By treatmentof this salt with a base (2R,3R)-thiomicamine is obtained asenantiomerically pure free base.

An acid is added to the mother liquors and they are heated forequilibrating the diastereomer (2R,3S) with that (2R,3R). The cycle isrepeated until thiomicamine terminates. Alternatively, further acid andfurther compound VI (2R,3S) may be added to the mother liquors thusrepeating both the hydrolysis and the equilibration.

An alternative procedure for carrying out step D consists in carryingout the hydrolysis (D-2) and perform subsequently the equilibration ofthe (2R,3S)-thiomicamine thus obtained.

The epimerization of the benzylic centre may be carried out according tothe following experimental conditions:

in acidic water, thereby isolating the salt of thiomicamine with theselected acid or thiomicamine as free base after alkalinization of thereaction mixture after epimerization;

in a carboxylic acid (acetic or propionic) as solvent, optionally in thepresence of a strong acid; ester or amides of thiomicamine are isolateddepending on the used concentration and amount of acid. Freethiomicamine is obtained by mild hydrolysis;

in an alcoholic medium (methanol or ethanol) in the presence of at leasta stoichiometric amount of a strong acid. In this case, if desired, anether derivative of thiomicamine with the used alcohol may be isolated(3-alkoxy-analog of thiomicamine) from which free thiomicamine isobtained by mild hydrolysis of the ether group. Alternatively, thehydrolysis may be carried out in the reaction mixture by a simpledilution of the epimerization mixture with water.

in a presently preferred embodiment, in an anhydride with a strong acid,in particular, in acetic anhydride and hydrated p.toluenesulphonic acid,followed by mild basic hydrolysis. It is likely that the reactioninvolves the formation of cyclic intermediates and also of acyloxyderivatives.

In fact, starting from(4R,5S)-2,2-dimethyl-3-acetyl-4-hydroxymethyl-5-(4-methylthiophenyl)-1,3-oxazolidineas compound VI and by operating in the above conditions, theintermediates(4R,5S)-2,2-dimethyl-3-acetyl-4-acetoxymethyl-5-(4-methylthiophenyl)-1,3-oxazolidineand(4R,5R)-2-methyl-3-acetyl-4-acetoxymethyl-5-(4-methylthiophenyl)2-oxazolinewere isolated.

The above reported reactions afford (2R,3R)-thiomicamine i.e. compound I(2R,3R) wherein X=CH₃ S. In an analogous way step D is carried out forobtaining the compound of formula I (2R,3R) wherein X=H.

When it is desired to prepare the compounds of formula I havingconfiguration (2R,3R) in which X=CH₃ SO₂, CH₃ SO or NO₂ it is necessaryto carry out step D in a different way.

The inversion of the carbon atom in 3 (benzylic centre) is carried outby an S_(N) 2 nucleophilic substitution.

The compound VI (2R,3S) is firstly subjected to a mild hydrolysis fordeprotecting the benzylic hydroxy while leaving the nitrogen protectedas amide. The CH₂ OH group is protected as an ester by reaction with anacyl halide in the presence of a base thus obtaining a compound offormula IV-A but having 2R,3S configuration. This is then treated withthionyl chloride in dichloromethane and the reaction product issubjected to a complete hydrolysis. Also in this case, it is likely thatthe reaction involves the formation of an oxazoline intermediate.

An alternative procedure consists in treating with a base directly thecompound VI (2R,3S) i.e. without having deprotected the benzylichydroxy. The desired product is then obtained by deprotecting thefunctional group by mild hydrolysis in an acidic medium.

The above described process thus allows, through the four steps A, B, Cand D, the inversion of both the asymmetric carbon atoms of molecules offormula II, but also starting from erythro forms.

This result is possible thanks to a double inversion which is realizedby means of two sequential reciprocal inductions. In the first inversionthe benzylic carbon atom induces the preferential configuration of thecarbon in position 2 bound to the nitrogen and to the oxidized group, inthe subsequent induction the carbon atom having R configuration inposition 2 induces configuration R during the equilibration of thebenzylic carbon atom.

It is worth noting how the reactions involved in the process afford highyields and need cheap reactants of normal industrial use. Moreover, ascited at the beginning of the specification, the process is easilysuitable for the preparation of(2S,3R)-3-(4-methyl-thiophenyl)-3-hydroxy-2-amino-1-fluoro-propane andof the analog 3-(4-methylsulphonylphenyl)-derivative which are usefulintermediates for the synthesis of Florfenicol (European patent 14437).It must be again recalled that by nomenclature conventions the presenceof the fluorine atom instead of the hydroxy causes a change in thedenomination of the carbon atom in position 2 (from R to S) but it doesnot correspond to a variation in the configuration. In European patentapplication No. 130633 (Zambon S.p.A.) a process for the preparation ofFlorfenicol is described, said process comprises the replacement of thehydroxy by a fluorine atom in cyclic intermediates among which alsooxazolidines and 1,3-oxazolidine-2-ones.

The process object of the invention may be applied to the synthesis ofFlorfenicol by the following procedure.

After having carried out the inversion of the asymmetric centre in 2 andthe reduction of the formyl (or alkoxycarbonyl) group to hydroxymethyl,i.e. after having performed steps A, B and C, the CH₂ OH group of thereaction product [VI (2R,3S)] is transformed into CH₂ F. Thetransformation is carried out according to what described in Europeanpatent application No. 130633 above cited and preferably by a mesylationof the hydroxy and reaction of the mesylated product with KF inpolyglycol.

The compound of formula ##STR10## wherein R₂, R₅ and R₆ have the abovereported meanings, is thus obtained.

By carrying out step D of the process on compound VII, the inversion ofthe benzylic centre and the deprotection from the protective groups isrealized thus obtaining the(2S,3R)-3-(4-methylthiophenyl)-3-hydroxy-2-amino-1-fluoro-propane fromwhich, by a known method Florfenicol is prepared. It is likely that theintermediates of the process comprise oxazoline derivatives as abovediscussed.

Also in this case it is possible to perform the process starting from4-methylsulphonyl-derivatives (II, X=CH₃ SO₂) or to prepare thecorresponding intermediate by oxidation of the CH₃ S group to CH₃ SO₂ incompound VII.

The epimerization of the benzylic centre in 3 will be then performed byan S_(N) 2 nucleophilic substitution as above reported.

As above mentioned, in the specific cases of the compounds of formula IIwherein X=H or CH₃ S it is possible to perform the general process abovedescribed by inverting the order of some of the steps. It has been infact surprisingly observed that by treatment with carboxylic acidsoptionally in the presence of a strong acid or with acidic water, thecompounds of formula II wherein X=H or CH₃ S undergo an inversion ofconfiguration at the benzylic carbon atom in 3 which affords athermodynamic equilibrium mixture wherein the compound II (2S,3R) may beseparated in the form of triacyl-derivative (diester-amide) and this byhydrogenolysis affords the compound II (2S,3R) or its correspondingamide.

This allows to realize an alternative of the process object of theinvention wherein the inversion of the benzylic centre in 3 is notperformed during step D but precedes step A.

Said process may be summarized as follows:

D-1) Epimerization of the benzylic centre in 3 to obtain compound

II wherein X=H or CH₃ S having configuration (2S,3R).

A) Protection of the amino and hydroxy group in position 3 of theproduct from step D-1.

B) Oxidation of the CH₂ OH group to formyl, carboxy orcarboxy-derivative and epimerization of the carbon atom in alpha to theoxidized group.

C) Restoring of the primary alcoholic function by reduction of theoxidized group.

D-2) Deprotection from the protective groups introduced in step A. StepD-1 is carried out, as above reported, by treating compound II (2S,3S)wherein X=H, CH₃ S with an acid in epimerization conditions. By apractical point of view this is realized by heating a suspension ofcompound II in water in the presence of a strong acid or by heating asolution of compound II in acetic or propionic acid optionally in thepresence of a strong acid.

Step D-1, thus, is completely analog to step D in its feature concerningthe epimerization of the benzylic centre in 3, the only difference beingthe fact that the inversion of the carbon atom in 2 bound to the aminogroup did not yet occur.

Compound II (2S,3R) (X=H, CH₃ S) thus obtained is then reacted accordingto steps A, B and C which afford the inversion of the carbon atom in 2.

Steps A, B and C are carried out exactly as above reported. Obviously,having already inverted the configuration of the carbon atom in 3, theconfiguration of same in the intermediates III-A, III-B, IV-A, IV-B, Vand VI is inverted.

Step D-2 than follows and is carried out according to what described forstep D in its feature concerning the removal of the protective groupsintroduced in step A.

Also in this case, obviously, the hydrolysis reactions must be performedin mild conditions in order to avoid epimerization of the stereogeniccentres.

The use of acidic water as reaction medium is again useful provided thatthe temperature and the reaction time be sufficient for carrying out thetwo hydrolysis but do not give substantial epimerization.

In a practical embodiment, which is presently the preferred for theinversion of the two stereogenic centres of thiomicamine, the processobject of the invention comprises the following steps:

condensation of 2S,3S-thiomicamine with acetone to afford(4S,5S)-5-(4-methylthiophenyl)-4-hydroxymethyl-2,2-dimethyl-1,3-oxazolidineand N-acetylation of same;

oxidation of the hydroxymethyl group to formyl and epimerization of thecarbon atom in 4 of the oxazolidine;

reduction of the formyl to hydroxymethyl by NaBH₄ ;

treatment with an acid in an aqueous medium for epimerizing the carbonatom adjacent to the phenyl and for deprotecting the(2R,3R)-thiomicamine;

followed by the recycling of the mother liquors of the last reaction.

In a still more preferred embodiment, the last step is carried out byusing acetic anhydride with hydrated p.toluenesulphonic acid. This lastreaction is quite new and unexpected.

It is worth noting that the process object of the invention takeadvantage of some per se known reactions together with some new andunexpected reactions and results.

Certain reactions like protection and deprotection of functional groups,oxidation of primary alcohols to carbonyl or carboxy derivatives andtheir reduction to alcohols are certainly per se known.

However, they are generally known as far as isolated functional groupsare concerned while the starting products and intermediates of theprocess contain contemporaneously various functional groups with severalpossibilities of interference.

For example, in the protection and oxidation steps there are threedifferent functional groups to discriminate, i.e. the primary hydroxy,the benzylic hydroxy and the amino group. Moreover, when in the startingproduct and intermediates X=CH₃ S, the sulphur atom too might beinvolved in the oxidation processes.

The starting product and the intermediates contain two adjacentasymmetric carbon atoms on a total of three carbon atoms of thealiphatic chain moreover, as a consequence, four stereoisomers existamong which it is necessary to discriminate for the realization of theprocess.

A further difficulty which had to be overcome was that of finding asynthetic strategy, and realize it in practice, by which could allow theepimerization of the carbon atom in 2 bound to the amino group whilekeeping unaltered the configuration of the benzylic carbon in 3 andsubsequently the epimerization of the benzylic carbon atom while keepingunaltered the configuration of the carbon atom in position 2.

The global strategy of the process was realized in practice thanks tocertain unexpected results like the finding of the quite unusual secondorder asymmetric transformation of which take advantage step B.

The epimerization of step D, to our knowledge, finds no precedent in theliterature and the preferred conditions (acetic anhydride and hydratedp.toluenesulphonic acid) are quite new too.

The most valuable merit of the process consists in having realized thefound strategy by using rather unexpensive and industrially availablereactants and by using reaction conditions which are easilyindustrialized.

With the aim to better illustrate the present invention the followingexample are given.

EXAMPLE 1

Preparation ofthreo-(2S,3S)-3-(4-methylthiophenyl)-3-hydroxy-2-acetamido-1-acetoxy-propane(Compound 1)

Triethylamine (104.5 g; 1.03 mol) was added at 25° C. in 15 minutes to asuspension ofthreo-(2S,3S)-2-amino-3-(4-methylthiophenyl)-1,3-propanediol[(2S,3S-thiomicamine] (100 g; 0.469 mol) in methylene chloride (500 ml)kept under mechanical stirring and under nitrogen, and then acetylchloride (81.1 g; 1.03 mol) was added dropwise in 2 hours. During theaddition the reaction temperature rose up to 40° C. At the end of theaddition the reaction mixture was cooled at 25° C. and kept understirring for 2 hours.

The reaction mixture was then poured into a 5% sodium bicarbonatesolution (500 ml); after separation of the phases, the aqueous phase wasextracted with methylene chloride (200 ml).

The combined organic phases were dried over sodium sulphate andevaporated to dryness under vacuum.

Crude compound 1 (140.2 g) (titre 67.4%) was obtained.

By column chromatography (silica gel, eluent ethylacetate:methanol=98:2) an analytically pure sample was obtained.

¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.91 (s, 3H); 2.08 (s, 3H); 2.47 (s,3H); 4.06 (dd, J=5.5 Hz, J=10.4 Hz, 1H); 4.26 (dd, J=10.4 Hz, J=6.2 Hz,1H); 4.30 (dddd, J=5.5; 6.2; 4.0; 8.1 Hz, 1H); 4.80 (d, J=4.0 Hz, 1H);6.01 (d, J=8.1 Hz, 1H); 7.13 (AA'BB'sy, Δν=20.9 Hz, 4H). I.R. (KBr):3450 cm⁻¹, 3380 cm⁻¹, 1750 cm⁻¹, 1655 cm⁻¹, 1635 cm⁻¹. M.p.=98.5°-99.5°C.

EXAMPLE 2

Preparation of(4S,5S)-5-(4-methylthiophenyl)-4-acetoxymethyl-3-acetyl-2,2-dimethyl-1,3-oxazolidine(Compound 2) and of(4S,5S)-5-(4-methylthiophenyl)-4-hydroxymethyl-3-acetyl-2,2-dimethyl-1,3-oxazolidine(Compound 3)

2,2-Dimethoxy-propane (355.4 g; 3.41 mol) and monohydratedp-toluenesulphonic acid (4.5 g; 0.02 mol) were added to a solution ofthe crude compound 1 (Example 1) (140 g) in acetone (275 ml) kept understirring and under nitrogen at 25° C.

The solution was heated under reflux for 1.5 hours and cooled to 25° C.Potassium carbonate (3.5 g; 0.02 mol) was added under stirring to thesolution. After 30 minutes the suspension was filtered and evaporatedunder vacuum to give an oily residue (161.3 g) (compound 2).

HPLC titre=53.2% By column chromatography (silica gel, eluent ethylacetate) an analytically pure sample was obtained.

¹ H-NMR (300 MHz, DMSO): δ(ppm): 1.48 (s, 3H); 1.51 (s, 3H); 2.04 (s,3H); 2.10 (s, 3H); 2.48 (s, 3H); 4.26 (m, J=4.34 Hz, 2H); 4.38 (m,Δν=13.9 Hz, 1H); 5.05 (d, J=4.0 Hz, 1H); 7.34 (AA'BB'sy, Δν=42.5 Hz,4H). I.R. (CCl₄): 2980 cm⁻¹, 1748 cm⁻¹, 1665 cm⁻¹, 1390 cm⁻¹, 1220 cm⁻¹.An 85% potassium hydroxide solution (31.7 g) in methanol (150 ml) wasadded in 1 hour into a solution of the crude compound 2 (161 g) inmethanol (500 ml) kept under mechanical stirring under nitrogen at 15°C.

The reaction mixture was evaporated to dryness and the residue wascollected by methylene chloride (400 ml) and a 2% ammonium chloridesolution (200 ml).

The aqueous phase was extracted with methylene chloride (100 ml); thecombined organic phases were washed with water, dried and evaporated todryness. A crude product (108.5 g) (HPLC titre 73.7%) was obtained whichwas crystallized from ethyl acetate (160 ml) to give compound 3 (50.9 g;173 mmol).

¹ H-NMR (300 MHz, DMSO): δ(ppm): 1.47 (s, 3H); 1.50 (s, 3H); 2.06 (s,3H); 2.47 (s, 3H); 3.55 (ddd, J=5.7; 11.5; 4.0 Hz, 1H); 3.61 (ddd,J=5.7; 11.5; 6.8 Hz, 1H); 4.06 (ddd, J=3.8 Hz, J=4.0 Hz, J=6.8 Hz, 1H);5.07 (d, J=3.8 Hz, 1H); 5.24 (t, J=5.7 Hz, 1H); 7.33 (AA'BB'sy, Δν=41.6Hz, 4H). [α]_(D) ²⁰ =+16.93° (conc. 1.06%, CHCl₃) I.R. (KBr): 3280 cm⁻¹,1630 cm⁻¹. M.p.=142°-145° C.

EXAMPLE 3

Preparation of(4R,5S)-5-(4-methylthiophenyl)-4-formyl-3-acetyl-2,2-dimethyl-1,3-oxazolidine(Compound 4)

A solution of dimethylsulphoxide (38.2 g; 0.49 mol) in methylenechloride (100 ml) was added to a solution of oxalyl chloride (23.21 g;0.183 mol) in methylene chloride (100 ml) kept at -60° C. undernitrogen. After 30 minutes a solution of compound 3 (Example 2) (50.9 g;0.173 mol) in methylene chloride (660 ml) was added. The reactionmixture was kept at -60° C. for 30 minutes, then triethylamine (91.0 g;0.96 mol) was added at -60° C. under stirring.

The reaction mixture was kept at -60° C. for minutes, then it was heatedto 0° C. in 1 hour and poured into a 5% sodium bicarbonate solution (350ml). The aqueous phase was washed with methylene chloride (100 ml); thecombined organic phases were dried over sodium sulphate and evaporatedunder vacuum to give an oily residue (53.7 g).

Compound 4

Major rotamer (56%) ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.62 (s, 3H); 1.70(s, 3H); 2.16 (s, 3H); 2.42 (s, 3H); 4.35 (dd, J=8.79-2.91 Hz, 1H); 4.91(d, J=8.79 Hz, 1H); 7.21 (AA'BB'sy, Δν=12.3 Hz, 4H); 9.50 (d, J=2.91 Hz,1H).

Minor rotamer (44%) ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.74 (s, 3H); 1.88(s, 3H); 2.16 (s, 3H); 2.43 (s, 3H); 4.28 (dd, J=6.83 Hz, J=2.93 Hz,1H); 5.06 (d, J=6.83 Hz, 1H); 7.24 (AA'BB'sy, Δν=19.8 Hz, 4H); 9.61 (d,J=2.93 Hz, 1H). I.R. (CCl₄): 2980 cm⁻¹, 1732 cm⁻¹, 1732 cm⁻¹, 1673 cm⁻¹,1495 cm⁻¹, 1395 cm⁻¹, 1350 cm⁻¹, 1250 cm⁻¹.

EXAMPLE 4

Preparation of(4S,5S)-5-(4-methylthiophenyl)-4-formyl-3-acetyl-2,2-dimethyl-1,3-oxazolidine(Compound 5)

1,4-Diazabicyclooctane (1.44 g; 0.0128 mol) was added to compound 4(53.7 g; 0.182 mol) kept under mechanical stirring at 30° C. undernitrogen. The mixture was heated to 40° C.

The reaction was monitored by ¹ H-NMR; as soon as the ratio betweencompounds 4 and 5 was equal to 50:50, the reaction mixture was seededwith crystallized compound 5 (30 mg).

The reaction mixture became heterogeneous due to the precipitation ofcompound 5.

At the end of the reaction (ratio 5:4=95:5) the suspension was dissolvedinto methylene chloride (500 ml) and the organic phase was washed withammonium chloride (2×20 ml). The organic phase was dried over sodiumsulphate and evaporated under vacuum. The residue (53.7 g) was used ascrude in the following step.

A sample crystallized by a mixture of isopropanol/isopropyl ether inratio 20:80 afforded the compound 5.

Major rotamer (93%) ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.73 (s, 3H); 1.85(s, 3H); 1.93 (s, 3H); 2.48 (s, 3H); 4.49 (dd, J=2.8 Hz, J=6.4 Hz, 1H);5.46 (d, J=6.4 Hz, 1H); 7.27 (AA'BB'sy, Δν=22 Hz, 4H); 9.17 (d, J=2.8Hz, 1H).

Minor rotamer (7%) ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.64 (s, 3H); 1.89(s, 3H); 2.23 (s, 3H); 2.47 (s, 3H); 5.00 (d, J=7.0 Hz, 1H); 5.36 (d,J=7.0 Hz, 1H); 7.27 (AA'BB'sy, Δν=22 Hz, 4H); 9.06 (s, 1H). I.R. (KBr):1735 cm⁻¹, 1660 cm⁻¹, 1645 cm⁻¹. M.p.=97°-102° C.

EXAMPLE 5

Preparation of(4R,5S)-5-(4-methylthiophenyl)-4-hydroxymethyl-3-acetyl-2,2-dimethyl-1,3-oxazolidine(Compound 6)

Calcium chloride (14.25 g; 0.13 mol) and sodium borohydride (4.95 g;0.13 mol) were added to a solution of the crude compound 5 (53.7 g; 0.18mol) in ethanol (570 ml) and tetrahydrofurane (220 ml) kept undermechanical stirring at -5° C. under nitrogen. After 2 hours the reactionwas poured into a pH 7 buffered phosphate solution (100 ml) andextracted with methylene chloride (2×300 ml). The collected organicphases were dried over sodium sulphate and evaporated under vacuum togive a residue (44.7 g; 95% compound 6, 5% compound 3) which wascrystallized from toluene. 35.0 g of 99% pure compound 6 were obtained.

¹ H-NMR (300 MHz, DMSO): δ(ppm): 1.58 (s, 3H); 1.62 (s, 3H); 2.10 (s,3H); 2.46 (s, 3H); 3.03 (ddd, J=11.2 Hz, J=5.1 Hz, J=5.3 Hz, 1H); 3.18(ddd, J=11.2 Hz, J=8.0 Hz, J=5.3 Hz, 1H); 4.25 (ddd, J=5.0 Hz, J=8.0 Hz,J=5.1 Hz, 1H); 4.65 (t, J=5.3 Hz, 1H); 5.25 (d, J=5.0 Hz, 1H); 7.27(AA'BB'sy, Δν=30.6 Hz, 4H). I.R. (KBr): 3320 cm⁻¹, 1630 cm⁻¹.M.p.=123°-128° C.

EXAMPLE 6

Preparation of Compound 6 from Compound 5 (alternative method)

Sodium borohydride (32.2 mg; 0.85 mmol) was added to a solution of purecompound 5 (250 mg; 0.85 mmol) in isopropanol (7.7 ml) kept undermechanical stirring at -20° C. under nitrogen. After 2 hours thereaction was poured into a pH 7 buffered phosphate solution (10 ml) andextracted with methylene chloride (2×50 ml). The combined organic phaseswere dried over sodium sulphate and evaporated under vacuum to give thecompound 6 having the same characteristics shown in example 5.

EXAMPLE 7

Preparation of compound 6 from compound 5 (alternative method)

Sodium borohydride (0.52 g, 13.65 mmol) and calcium chloride (1.52 g;13.65 mmol) were added to a solution of pure compound 5 (4 g; 13.65mmol) in absolute ethanol (42.7 ml) and tetrahydrofurane (16 ml) keptunder stirring at -5° C. under nitrogen. After 20 minutes the reactionwas poured into a buffered phosphate solution (10 ml) (KH₂ PO₄ /K₂ HPO₄=1:1 mol in 1 l) at pH 7 and extracted with methylene chloride (2×20ml). The organic phase was dried and the solvent was removed undervacuum up to residue (compound 6 having the same characteristics shownin the example 5).

EXAMPLE 8

Preparation of (2R,3R)-3-(4-methylthiophenyl)-2-amino-1,3-propanediol[(2R,3R)-thiomicamine]

Monohydrated p-toluenesulphonic acid (20 g; 105 mmol) was added at 25°C. under stirring to a suspension of compound 6 (10.0 g; 33.9 mmol) inwater (60 ml). The suspension was heated to 75° C. for 2.5 hours; thesolid dissolved in solution. The solution was heated to 95° C. and keptat this temperature for 42 hours. The solution was then cooled to 15° C.and during the cooling the p-toluenesulphonate of 2R,3R-thiomicamineprecipitated.

After 1 hour the solid was filtered at 15° C. and washed with water (20ml).

Sodium hydroxide (1.2 g) was added to the solid suspended in water (40ml) at 25° C., up to pH 10.5. From the solution, which was cooled to 5°C., 2R,3R-thiomicamine precipitated and was filtered, washed with water(20 ml) and dried in oven at 60° C. for 4 hours (4.3 g; 97% HPLC titre,92% diastereomeric excess). The solid was crystallized from isopropanol(100 ml) at 5° C. 3.4 g of pure 2R,3R-thiomicamine were obtained([α]_(D) ²⁰ =-33.8°, 99.8% HPLC titre, 99% diastereomeric excess).

EXAMPLE 9

Preparation of Compound 3 (see Example 2)-alternative method

A suspension of (2S,3S)-thiomicamine (100 g; 0.469 mol) in toluene (920ml) and acetone (100 ml) was heated under reflux under stirring for 18hours in a flask equipped reflux condenser and dean stark trapp, 10.6 gof a mixture containing acetone (3.9 g), water (6.6 g) and toluene (0.1g) were separated. At the end the solvent was evaporated under vacuum.(4S,5S)-5-(4-methylthiophenyl)-4-hydroxymethyl-2,2-dimethyl-1,3-oxazolidine(compound 7) (117 g) was obtained which was directly used for thefollowing step.

Compound 7:

¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.51 (s, 3H); 1.52 (s, 3H); 2.46 (s,3H); 3.17 (ddd, J=8.43 Hz, J=4.10 Hz, J=3.48 Hz, 1H); 3.62 (dd, J=4.10Hz, J=11.1 Hz, 1H); 3.80 (dd, J=3.48 Hz, J=11.1 Hz, 1H); 4.62 (d, J=8.17Hz, 1H); 7.24 (AA'BB'sy, Δν=21.8 Hz, 4H).

Acetyl chloride (29.4 g; 0.375 mol) was added in 2 hours to a solutionof compound 7 (90.38 g; 0.36 mol) in methylene chloride (900 ml) andtriethylamine (54.2 g; 0.54 mol) kept under stirring at 15° C. inertatmosphere.

The reaction mixture was then worked up by adding a 10% ammoniumchloride solution (200 ml). After separation of the phases, the aqueousphase was extracted with methylene chloride (200 ml). The combinedorganic phases were dried over sodium sulphate and evaporated todryness.

Potassium carbonate (24.8 g; 0.18 mol) was added to a solution of theresidue in methanol (300 ml) kept under stirring at 25° C. After 1 hourthe solvent was evaporated under vacuum and the residue was dissolved inmethylene chloride (300 ml). The solution was washed with water, driedover sodium sulphate and evaporated to dryness. A residue was obtainedwhich, crystallized from ethyl acetate, afforded the pure compound 3 (69g; 0.234 mol; 65% yield) having the same characteristics shown in theexample 2.

EXAMPLE 10

Preparation of(2S,3S)-3-(4-methylthiophenyl)-3-ethoxy-2-amino-propan-1-ol (Compound 8)and of (2S,3S)-3-(4-methylthiophenyl)-3-ethoxy-2-acetamido-propan-1-ol(Compound 9)

96% Sulphuric acid (d=1.835) (18.4 g; 10 ml; 187.6 mmol) was added understirring at room temperature to a suspension of (2S,3S)-thiomicamine (10g; 46.9 mmol) in ethanol (70 ml).

The mixture was heated to 90° C. for 0.5 hours, cooled to roomtemperature and poured into a sodium hydroxide solution (15 g; 375 mmol)in water (200 ml) to pH 10-11.

The compound 8 thus obtained was extracted with methylene chloride(2×300 ml), dried over sodium sulphate, evaporated to dryness and usedas crude in the following step.

Triethylamine (8.3 g; 82.22 mmol) and acetyl chloride (6.45 g; 82.22mmol) were added under stirring at room temperature and under nitrogento a solution of crude compound 8 (18.5 g; 82.22 mmol) in methylenechloride (92.5 ml).

After 15 minutes the reaction was poured into a 10% sodium bicarbonatesolution (100 ml). The aqueous phase was extracted with methylenechloride (100 ml); the combined organic phases were dried over sodiumsulphate and evaporated to dryness.

The residue (15.62 g) (compound 9) thus obtained was purified by columnchromatography (silica gel, eluent:ethyl acetate).

¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.19 (t, J=7.0 Hz, 3H); 1.94 (s, 3H);2.47 (s, 3H); 3.35 (dq, J=9.45 Hz, J=7.0 Hz, 1H); 3.47 (dq, J=9.46 Hz,J=7.0 Hz, 1H); 3.63 (dd, J=12; 5.1 Hz; 1H); 3.65 (dd, J=12.9 Hz; 1H);4.01 (dddd, J=7.3; 9.2; 5.1; 4.0 Hz; 1H); 4.55 (d, J=4 Hz, 1H); 6.09 (d,J=7.8 Hz, 1H); 7.20 (AA'BB'sy, Δν=20 Hz, 4H). I.R. (CCl₄): 3450 cm⁻¹,2980 cm⁻¹, 2930 cm⁻¹, 2880 cm⁻¹, 1495 cm⁻¹, 1095 cm⁻¹.

EXAMPLE 11

Preparation of(2R,3S)-3-(4-methylthiophenyl)-3-ethoxy-2-acetamido-1-propanale(Compound 10) and of the (2S,3S) diastereomer thereof (Compound 11)

A solution of dimethylsulphoxide (780 mg; 9.99 mmol) in methylenechloride (1 ml) was added to a solution of oxalyl chloride (475 mg; 3.74mmol) in methylene chloride (4 ml) kept at -60° C. under nitrogen. After30 minutes a solution of compound 9 (1.0 g; 3.53 mmol) in methylenechloride (7 ml) was added. The reaction mixture was kept at -60° C. for30 minutes, then a solution of triethylamine (1.86 g; 18.4 mmol) inmethylene chloride (2 ml) was added at -60° C. under stirring.

The reaction mixture was kept at -60° C. for 15 minutes, then was heatedto 0° C. in 1 hour and poured into a 5% sodium bicarbonate solution (10ml). The aqueous phase was washed with methylene chloride (30 ml); thecombined organic phases were dried over sodium sulphate and evaporatedunder vacuum to give an oily residue (505 mg).

The reaction directly afforded an equilibrium mixture of two epimercompounds (Compound 10 and 11).

Major diastereomer: ¹ H-NMR (300 MHz, CDCl₃); δ(ppm): 1.18 (t, J=7.0 Hz,3H); 1.99 (s, 3H); 2.47 (s, 3H); 3.44 (m, Δν=70 Hz, 2H); 4.75 (dd, J=3.9Hz, J=7.4 Hz, 1H); 4.95 (d, J=3.9 Hz, 1H); 6.11 (d, J=7.4 Hz, 1H); 7.17(AA'BB'sy, Δν=32 Hz, 4H); 9.77 (s, 1H).

Minor diastereomer: ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.16 (t, J=7.0 Hz,3H); 2.06 (s, 3H); 2.50 (s, 3H); 3.44 (m, Δν=70 Hz, 2H); 4.73 (dd, J=3.7Hz, J=7.4 Hz, 1H); 4.75 (d, J=3.7 Hz, 1H); 6.38 (d, J=7.4 Hz, 1H); 7.32(AA'BB'sy, Δν=30.9 Hz, 4H); 9.53 (s, 1H).

EXAMPLE 12

Preparation of(2R,3S)-3-(4-methylthiophenyl)-3-ethoxy-2-acetamido-propan-1-ol(Compound 12)

Calcium chloride (24 mg; 0.22 mmol) and sodium borohydride (12.3 mg;0.33 mmol) were added to a mixture of compounds 10 and 11 (50 mg; 0.0177mmol) in ethanol (0.34 ml) and tetrahydrofurane (0.22 ml) kept undermechanical stirring at -5° C. under nitrogen. After 2 hours the reactionwas poured into a pH 7 buffered phosphate solution (10 ml) and extractedwith methylene chloride (2×20 ml). The combined organic phases weredried over sodium sulphate and evaporated under vacuum to give a residuewhich was crystallized from toluene. 50 mg of a mixture formed bycompound 12 and its (2S,3S) diastereomer in ration 1:1 were obtained.

¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.22 (t, J=6.5 Hz, 3H); 2.08 (s, 3H);2.49 (s, 3H); 3.45 (m, Δν=90 Hz, 2H); 3.87 (dd, J=2.3, J=11.3, 1H); 3.93(m, Δν=15 Hz, 1H); 4.3 (m, Δν=18 Hz, 1H); 4.71 (d, J=3.1 Hz, 1H); 6.44(d, J=6.6 Hz, 1H); 7.28 (ABsy, Δν=32 Hz, 4H).

EXAMPLE 13

Preparation of(2R,S,4S,5S)-5-(4-methylthiophenyl)-4-acetoxymethyl-3-acetyl-2-methoxy-1,3-oxazolidine(Compound 13)

Monohydrated paratoluenesulphonic acid (16.2 mg) to a mixture ofcompound 1 (see Example 1), trimethylorthoformiate (5 ml), heated to 40°C. under stirring.

The reaction mixture was kept under stirring at 40° C. for 1 hour andthen poured into 8% NaHCO₃ and extracted with CH₂ Cl₂ (2×25 ml). Thecombined organic phases were dried.

By removing the solvent under vacuum a residue (510 mg) principallyformed by compound 13 was obtained.

EXAMPLE 14

Preparation of(2R,S,4S,5S)-5-(4-methylthiophenyl)-4-hydroxymethyl-3-acetyl-2-methoxy-1,3-oxazolidine(Compound 14)

NaOH (1.42 g) was added under stirring at room temperature to a solutionof compound 13 (210 mg; 0.65 mol) in CH₃ OH (3 ml). It was kept understirring for 30 minutes, poured into water and extracted with methylenechloride (2×25 ml). By evaporation of the combined organic extracts thecompound 14 was obtained.

¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 2.2 (s, 3H); 2.48 (s, 3H); 3.46 (s,3H); 3.74 (dd, J=6.3 Hz, J=12.0 Hz, 1H); 3.83 (dd, J=2.0 Hz, J=12.0 Hz,1H); 3.96 (ddd, J=6.3 Hz, J=2.0 Hz, J=8.7 Hz, 1H); 4.92 (d, J=8.7 Hz,1H); 5.97 (s, 1H); 7.28 (ABsy, Δν=20 Hz, 4H).

EXAMPLE 15

Preparation of(4S,5S)-5-(4-methylthiophenyl)-4-benzoyloxymethyl-3-benzoyl-2,2-dimethyl-1,3-oxazolidine(Compound 15)

Benzoyl chloride (56 g; 0.41 mol) was added without exceeding thetemperature of 5° C. to a mixture of compound 7 (see Example 9) (50 g;0.198 mol) in methylene chloride (250 ml) and triethylamine (42 g; 0.42mol) cooled to 0° C.

After 1 hour from the end of the addition, the reaction mixture waspoured into water (200 ml). The phases were separated and the organicphase was dried over sodium sulphate and evaporated to residue undervacuum. 78 g of compound 15 were obtained.

¹ H-NMR (300 MHz, DMSO): δ(ppm): 1.7 (s, 6H); 2.49 (s, 3H); 4.00 (2H);4.29 (1H); 5.12 (d, 1H, J=7.6 Hz); 7.28-7.85 (14H, aromatics).

EXAMPLE 16

Preparation of(4S,5S)-5-(4-methylthiophenyl)-4-hydroxymethyl-3-benzoyl-2,2-dimethyl-1,3-oxazolidine(Compound 16 )

A mixture of compound 15 (70 g; 0.15 mol), methanol (500 ml), K₂ CO₃ (22g; 0.16 mol), was stirred at room temperature for 1 hour. The insolublesalts were filtered and it was evaporated under vacuum to dryness.

The residue was dissolved into methylene chloride (200 ml), the solutionwas washed with water (2×100 ml). The organic phase was dried oversodium sulphate and the solvent was evaporated under vacuum to give aresidue (55 g) principally formed by compound 16.

¹ H-NMR (300 MHz, DMSO): δ(ppm): 1.68 (s, 6H); 2.49 (s, 3H); 3.00 (2H);3.82 (1H); 5.07 (d, 1H, J=7.6 Hz); 7.27-7.5 (9H, aromatics). By columnchromatography on silica gel (eluent ethyl ether) of a sample the pureproduct was obtained with m.p.=128°-131° C.

EXAMPLE 17

Preparation of(4R,5S)-5-(4-methylthiophenyl)-4-formyl-3-benzoyl-2,2-dimethyl-1,3-oxazolidine(Compound 17)

A solution of DMSO (780 mg; 10 mmol) in CH₂ Cl₂ (10 ml) was added understirring and under nitrogen to a solution of oxalyl chloride (470 mg;3.70 mmol) in CH₂ Cl₂ (2 ml) cooled to -60° C.

The solution was stirred at -60° C. for 30 minutes. A solution ofcompound 16 (1.25 g; 3.5 mmol) in methylene chloride (8 ml) was added in15 minutes to the solution kept at -60° C. under stirring. The mixturewas kept under stirring at -60° C. for 15 minutes and then Et₃ N (2.1 g;2 ml) in methylene chloride (2 ml) was added to the solution.

The solution temperature was heated to 0° C. and the solution was pouredinto water (50 ml); the phases were separated and the organic phase,after drying over sodium sulphate, was evaporated under vacuum to give aresidue (1.35 g) formed by compound 17.

¹ H-NMR (300 MHz, DMSO): δ(ppm): 1.75 (6H); 2.48 (s, 3H); 4.47 (dd, 1H,J=8.3 Hz, J=3.5 Hz); 5.19 (d, 1H, J=8.3 Hz); 7.27-7.51 (9H, aromatics);9.14 (d, 1H, J=3.5 Hz).

EXAMPLE 18

Preparation of(4S,5S)-5-(4-methylthiophenyl)-4-methylsulphonyloxymethyl-3-benzoyl-2,2-dimethyl-1,3-oxazolidine(Compound 18)

Mesyl chloride (630 mg; 5.5 mmol) was added under stirring an undernitrogen at 0° C. to a solution of compound 16 (see Example 16) (1.5 g;9.2 mmol), Et₃ N (600 mg; 6 mmol) in CH₂ Cl₂ (7.5 ml). The mixture wasstirred at 0° C. for 1 hour, then poured into water (20 ml). The organicphase was dried over Na₂ SO₄ and the solvent was evaporated under vacuumto give a residue which was chromatographed on SiO₂ with Et₂ O to affordthe compound 18 (800 mg).

¹ H-NMR (300 MHz, DMSO): δ(ppm): 1.66 (s, 6H); 2.49 (s, 3H); 3.13 (s,3H); 3.95 (m, 2H); 4.18 (ddd, 1H, J=7.6 Hz, J=3.91 Hz, J=2.63 Hz); 5.04(d, 1H, J=7.6 Hz); 7.30-7.55 (5H, aromatics).

EXAMPLE 19

Preparation of(2S,3R)-3-(4-methylthiophenyl)-2-acetamido-1,3-propanediol (Compound 19)

(2S,3S)-Thiomicamine (30 g; 0.141 mol) in acetic acid (130 ml) washeated under reflux (117° C.) for 23 hours.

Evaporation of the solvent under vacuum afforded a residue which wasdissolved into methanol (130 ml). Sodium hydroxide (14.6 g; 0.36 mol)was added at 15° C. to the thus obtained solution.

The reaction mixture was brought to pH 6.2 with hydrochloric acid andevaporated under vacuum.

The oily residue was dissolved into methylene chloride (80 ml) and water(100 ml).

After separation of the phases, the organic phase was dried over sodiumsulphate and evaporated to dryness.

The compound 19 (3.4 g; diastereomeric ratio 98:2) was obtained bycrystallization from ethyl acetate. ¹ H-NMR (300 MHz, CDCl₃): δ(ppm):1.73 (s, 3H); 2.47 (s, 3H); 3.63 (dd, J=7.5 Hz, J=3.5 Hz, 1H); 3.84 (dd,J=7.5 Hz, J=2.9 Hz, 1H); 4.06 (dddd, J=2.9 Hz, J=3.5 Hz, J=4.0 Hz, J=7.8Hz, 1H); 7.30 (ABsy, Δν=30 Hz). 300 mg of pure compound 19 were refluxheated for 5 hours with NaOH. By saturating the solution with NaCl(2S,3R)-thiomicamine precipitated. [α]_(D) ²⁵ =-26°-44°

EXAMPLE 20

Preparation of(4S,5S)-5-(4-methylthiophenyl)-4-formyl-3-acetyl-2,2-dimethyl-1,3-oxazolidine(Compound 5)

Pyrrolidine (9.6 mg; 0.065 mmol) was added at 25° C. to a solution ofcompound 4 (see example 3) (100 mg, 0.34 mmol) in toluene (2 ml) keptunder magnetic stirring and under nitrogen. At the end of the additionthe mixture was kept at 25° C. under stirring for 14 hours. The reactionmixture was then poured into 10% NaHCO₃ ; after separation of thephases, the aqueous phase was extracted with CH₂ Cl₂. The combinedorganic phases were dried over sodium sulphate and evaporated to drynessunder vacuum.

A mixture of compound 4 and compound 5 in the ratio 38:62 was obtained.

EXAMPLE 21

Preparation of(4S,5S)-5-(4-methylthiophenyl)-4-hydroxymethyl-1,3-oxazolidine (Compound20)

Paraformaldehyde (1.48 g; 49.84 mmol) was added to a suspension of(2S,3S)-thiomicamine (10 g; 46.9 mmol) in toluene (60 ml).

The mixture was heated at reflux under magnetic stirring for 1.5 hourswhile distilling through a dean stark trapp.

The reaction mixture was cooled down and toluene was evaporated undervacuum up to an oily residue which was used without any purification inthe next reactions.

EXAMPLE 22

Preparation of(4S,5S)-5-(4-methylthiophenyl)-4-hydroxymethyl-3-acetyl-1,3-oxazolidine(Compound 21)

Triethylamine (560 mg; 5.55 mmol) and thereafter acetyl chloride (309mg; 3.93 mmol) were added to a solution of compound 20 (1 g; 3.7 mmol)in methylene chloride (10 ml).

After 1 hour a 10% sodium bicarbonate aqueous solution was added to thereaction mixture; the phases were separated and the organic one waswashed with a buffered phosphate solution having pH 7. The organicextract was dried over sodium sulphate and evaporated to dryness.

The crude thus obtained was chromatographed on silica gel using amixture of diethylether and ethylacetate.

Compound 21 was obtained pure in the form of two conformers (rotamers).

Major rotamer: ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.98 (s, 3H); 2.47 (s,3H); 3.59 (m, Δν=30 Hz, 2H); 3.86 (ddd, J=5.1 Hz, 5 Hz, 1H); 4.94 (d,J=4.2 Hz, 1H); 5.08 (d, J=5.1 Hz, 1H); 5.27 (d, J=4.2 Hz, 1H); 7.20-7.32(aromatic protons, 4H).

Minor rotamer: ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 2.00 (s, 3H); 2.47 (s,3H); 3.59 (m, Δν=30 Hz, 2H); 3.93 (ddd, J=3.6 Hz; J=5.81; J=5.81 Hz,2H); 4.75 (d, J=5.1 Hz, 1H); 5.08 (d, J=3.6 Hz, 1H); 5.30 (d, J=5.1 Hz,1H); 7.20-7.32 (aromatic protons, 4H).

EXAMPLE 23

Preparation of Compound 6 from Compound 5 (alternative method)

Compound 5 (500 mg) was added to a solution of acetic acid (24 mg) inethanol (10 ml).

Sodium borohydride (16 mg) was added under stirring to the solutioncooled to -5° C.

The solution was kept under stirring for 1 hour and then poured into apH 7 buffered aqueous solution and extracted with methylene chloride(2×25 ml).

The combined organic phases were washed with water and the solvent wasevaporated under vacuum to give compound 6 (500 mg) having the samecharacteristics shown in example 5.

EXAMPLE 24

Preparation of(2S,3S)-3-(4-methylthiophenyl)-3-methoxy-2-amino-propan-1-ol (Compound22) and of(2S,3S)-3-(4-methylthiophenyl)-3-methoxy-2-acetamido-propan-1-ol(Compound 23)

96% Sulphoric acid (d=1.835) (1.84 g; 1 ml; 18.77 mmol) was added atroom temperature under stirring to a suspension of (2S,3S)-thiomicamine(1 g; 4.69 mmol) in methanol (4.9 ml).

The mixture was heated at 90° C. for 0.5 hours, cooled to roomtemperature and poured into a solution of sodium hydroxide (1.5 g; 37.5mmol) in water (15 ml) to a pH of 10-11.

The (2S,3S)-3-(4-methylthiophenyl)-3-methoxy-2-amino-propan-1-ol(compound 22) thus obtained was extracted with methylene chloride (2×30ml), dried over sodium sulphate, evaporated to dryness and used in thefollowing step.

¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 2.47 (s, 3H); 2.83 (m, Δν=30 Hz, 1H);3.2 (s, 3H); 3.3 (dd, J=5.8 Hz, J=10.0 Hz, 1H); 3.42 (dd, J=10.0 Hz,J=3.6 Hz, 1H); 4.02 (d, J=6.9 Hz, 1H); 7.23 (ABsy, Δν=45 Hz, 4H).

Triethylamine (2.6 g; 26.43 mmol) and acetyl chloride (1.52 g; 19.4mmol) were added to a solution of crude compound 22 (2.0 g; 8.81 mmol)in methylene chloride (10 ml), under stirring at room temperature andunder nitrogen.

After 15 minutes the reaction was poured into a 10% sodium bicarbonateaqueous solution (10 ml). The aqueous phase was extracted with methylenechloride (10 ml); the combined organic phases were dried over sodiumsulphate and evaporated to dryness.

A residue (compound 23) was obtained, which was crystallized frommethylene chloride.

¹ H-NMR (300 MHz, DMSO): δ(ppm): 1.76 (s, 3H); 2.43 (s, 3H); 3.11 (s,3H); 3.17 (m, Δν=30 Hz, 1H); 3.43 (m, Δν=30 Hz, 1H); 3.87 (m, Δν=30 Hz,1H); 4.34 (d, J=4.60 Hz, 1H); 4.77 (t, J=6 Hz, 1H); 7.22 (ABsy, Δν=20Hz, 4H); 7.68 (d, J=10 Hz, 1H).

EXAMPLE 25

Preparation of(2R,3S)-3-(4-methylthiophenyl)-3-methoxy-2-acetamido-1-propanale(Compound 24)

A solution of dimethylsulphoxide (64 mg; 0.82 mmol) in methylenechloride (0.1 ml) was added to a solution of oxalyl chloride (40 mg;0.32 mmol) in methylene chloride (300 μl) kept at -60° C. undernitrogen. After 30 minutes a solution of compound 23 (80 mg; 3.53 mmol)in methylene chloride was added. The reaction mixture was kept at -60°C. for 30 minutes, then a solution of triethylamine (211 mg; 2 mmol) inmethylene chloride (2 ml) was added at 60° C. under stirring. Thereaction mixture was kept at -60° C. for 15 minutes, then was heated to0° C. in 1 hours and poured into a 5% sodium bicarbonate aqueoussolution (20 ml). The aqueous phase was washed with methylene chloride(30 ml); the combined organic phases were dried over sodium sulphate andevaporated under vacuum to give an oily residue (85 mg) (Compound 24). ¹H-NMR (300 MHz, DMSO): δ(ppm): 1.81 (s, 3H), 3.10 (s, 3H); 4.58 (dd,J=3.7 Hz, J=8.10 Hz, 1H); 4.92 (d, J=3.7 Hz, 1H); 7.24 (ABsy, Δν=45 Hz,4H); 8.22 (d, J=8.5 Hz, 1H); 9.56 (s, 1H).

EXAMPLE 26

Preparation of(4S,5S)-5-(4-methylthiophenyl)-4-hydroxymethyl-2,2-diethyl-1,3-oxazolidine(Compound 25)

By working as described in the example 9 and using 3-pentanone (100 ml)instead of acetone the compound 25 was obtained in quantitative yield.

¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 0.98 (t, J=7.5 Hz, 3H); 1.04 (t, J=7.5Hz, 3H); 1.76 (q, J=7.5 Hz, 2H); 1.80 (q, J=7.5 Hz, 2H); 2.47 (s, 3H);3.17 (ddd, J=8.8; 4.0; 3.5 Hz, 1H); 3.63 (dd, J=4.0; 11.3 Hz, 1H); 3.82(dd, J=3.5; 11.3 Hz, 1H); 4.62 (d, J=8.8 Hz, 1H); 7.20-7.34 (aromatics,4H). I.R. (film): 2970 cm⁻¹, 2920 cm⁻¹, 1600 cm⁻¹, 1500 cm⁻¹, 1205 cm⁻¹,1090 cm⁻¹, 1060 cm⁻¹.

EXAMPLE 27

Preparation of compound 4 (see Example 3)--alternative method

Dimethylsulphoxide (0.78 g; 10 mmol) was added under nitrogen to amixture of compound 3 (example 2) (1.18 g; 4 mmol) in methylene chloride(7.5 ml).

It was cooled to -15° C. and phosphoric anhydride (1.42 g; 10 mmol) wasadded to it.

The solution was kept at -15° C. under stirring for 0.5 hours.Triethylamine (2 g; 20 mmol) was slowly added dropwise. After 10 minutesfrom the end of the addition, the mixture was poured into water (50 ml);the phases were separated.

The organic phase was washed with a sodium chloride saturated solution(50 ml), dried over sodium sulphate, evaporated to residue to give 1.35g of a crude which was almost exclusively formed by the desired product(compound 4).

EXAMPLE 28

Preparation of compound 4 (see Example 3)--alternative method

Pyridine (1.6 g; 20 mmol) was added under nitrogen to a mixture ofcompound 3 (example 2) (1.18 g; 4 mmol) in methylene chloride (10 ml).

A solution of chlorine (4 mmol) in carbon tetrachloride was added atroom temperature to the previous solution.

It was kept at room temperature under stirring for 0.5 hours. Thereaction mixture was poured into water (50 ml); the phases wereseparated.

The organic phase was washed with 4N hydrochloric acid. The solution wasdried over sodium sulphate and evaporated to residue to give 1.36 g of acrude which was formed by the desired product (compound 4).

EXAMPLE 29

Preparation of compound 4 (see Example 3)--alternative method

A mixture of chromic anhydride (2.1 g), pyridine (3.2 g) and methylenechloride (50 ml) was added, at room temperature, under nitrogen, to asolution of compound 3 (example 2) (1 g) in methylene chloride (15 ml).

It was kept at room temperature under stirring for 15 minutes. Thesolution was decanted and the residue was washed with ethyl ether (2×30ml). The combined organic phases were evaporated to residue. The residuewas dissolved in methylene chloride (50 ml) and the solution was washedwith diluted hydrochloric acid.

The organic phase was washed with a sodium chloride saturated solution(50 ml), dried over sodium sulphate, evaporated to residue to give 0.8 gof a crude containing the desired product (compound 4).

EXAMPLE 30

Preparation of compound 4 (see Example 3)--alternative method

A solution prepared by dissolving compound 3 (example 2) (2.36 g; 8mmol) and triethylamine (0.8 g; 8 mmol) in methylene chloride (15 ml)was added in 20 minutes, under stirring, to a solution ofdimethylsulphide (0.62 g; 10 mmol) and chlorine (0.71 g; 10 mmol) cooledto -20° C.

It was kept at -20° C. under stirring for 0.5 hours. Triethylamine (2 g;20 mmol) was added dropwise. After 10 minutes from the end of theaddition, the reaction mixture was poured into water (50 ml); the phaseswere separated.

The organic phase was washed with a sodium chloride saturated solution(50 ml), dried over sodium sulphate, evaporated to residue to give 2.40g of a crude which was formed by the desired product (compound 4).

EXAMPLE 31

Preparation of compound 4 (see Example 3) from compound 3 (see Example2)

A) Chlorine (2.35 g; 33.1 mmol) was added under stirring to a mixture ofdimethylsulphide (2.17 g; 35 mmol) in methylene chloride (25 ml) cooledto -30° C. A solution of triethylamine (3 g; 30 mmol) and compound 3(8.85 g; 30 mmol) in methylene chloride (70 ml) was added dropwise tothe mixture kept at -20° C. A solution of triethylamine (7.6 g; 75 mmol)in methylene chloride (20 ml) was added dropwise in 30 minutes understirring to the reaction mixture kept at -20° C. At the end of theaddition the reaction mixture was heated to 0° C. and poured into water(150 ml). After separation of the phases the organic phase was driedover sodium sulphate and evaporated under vacuum to give an oily residue(9 g) containing 4.6 g of 4.

B) Trichlorocyanuric acid (4.6 g; 20 mmol) was added portionwise understirring to a mixture of compound 3 (5.9 g; 20 mmol) and pyridine (7.9g; 100 mmol) in methylene chloride (50 ml) cooled to 0° C. The mixturewas kept under stirring at 0° C. for 1 hour and then poured into water(150 ml). The organic phase was washed with 1N hydrochloric acid (120ml) and dried over sodium sulphate. The solvent was evaporated undervacuum to give 6 g of a residue containing 4.

C) Trichlorocyanuric acid (2.32 g; 10 mmol) was added portionwise to amixture of compound 3 (2.95 g; 10 mmol) and dimethylsulphide (0.68 g; 11mmol) in methylene chloride (29.5 ml) cooled to -20° C. Triethylamine(4.05 g; 40 mmol) was added dropwise under stirring to the mixture keptat -20° C. for 0.5 hours. At the end of the addition the mixture waspoured into water (100 ml); after separation of the phases, the organicphase was washed with 0.1N hydrochloric acid (50 ml) and dried oversodium sulphate. 3.9 g of a residue containing 4 were obtained.

D) Phosphoric anhydride (2.85 g; 20 mmol) was added portionwise understirring to a mixture of dimethylsulphoxide (2.34 g; 30 mmol),dimethylformamide (6 ml) and compound 3 (2.95 g; 10 mmol) cooled to 15°C., while the reaction mixture spontaneously warmed up to 50° C. Themixture was stirred for 2 hours at 50° C., cooled to 20° C. and pouredinto a mixture of water (50 ml) and methylene chloride (50 ml).

After separation of the phases the organic phase was dried over sodiumsulphate and evaporated to residue under vacuum. 4.5 g of a residuecontaining 2.1 g of 4 were obtained.

E) Phosphoric anhydride (4.3 g; 30 mmol) was added, portionwise and bykeeping the temperature between 0° and 5° C., to a mixture ofdimethylsulphoxide (11 g; 0.14 mol) and methylene chloride (6 ml).

Compound 3 (5.9 g; 20 mmol) was added portionwise under stirring in 30minutes to the mixture kept at 0° C. and after further 30 minutes,triethylamine (4.1 g; 40 mmol) was added in 1 hour. The reaction mixturewas poured into a mixture of water (50 ml) and methylene chloride (50ml). After separation of the phases the organic phase was dried oversodium sulphate and removed up to residue under vacuum. 6.5 g of aresidue containing 4 g of compound 4 were obtained.

F) Phosphoric anhydride (17 g; 0.12 mol) was added under stirring to asolution of dimethylsulphoxide (13.2 g; 0.169 mol), dimethylformamide(25 g) in methylene chloride (100 ml) cooled to 0° C. and after 30minutes compound 3 (17.5 g; 0.059 mol). Triethylamine (18 g; 0.18 mol)was added in 1 hour under stirring to the mixture while keeping thetemperature between 0° C. and 5° C. The mixture was poured into water(100 ml) and the organic phase was dried over sodium sulphate andevaporated to dryness under vacuum. 34.5 g of a residue containing 15 gof compound 4 were obtained.

G) Trichlorocyanuric acid (2.32 g; 10 mmol) was added portionwise understirring to a mixture of compound 3 (2.95 g; 10 mmol) in methylenechloride (29.5 ml) and methyl-phenyl-thioether (1.37 g; 11 mmol) cooledto -20° C. Triethylamine (4.05 g; 40 mmol) was added dropwise understirring to the mixture kept at -20° C. for 0.5 hours. At the end of theaddition the mixture was poured into water (100 ml) and after separationof the phases the organic phase was washed with 0.1N hydrochloric acid(50 ml), dried over sodium sulphate and evaporated under vacuum. 4.1 gof a crude containing compound 4 were obtained.

H) Trichlorocyanuric acid (2.32 g; 10 mmol) was added portionwise understirring to a solution of compound 3 (2.95 g; 10 mmol) in methylenechloride (29.5 ml) cooled to -20° C. Triethylamine (4.05 g; 40 mmol) wasadded dropwise to the mixture kept under stirring at -20° C. for 0.5hours. The mixture was poured into water (100 ml) and after separationof the phases the organic phase was dried over sodium sulphate andevaporated under vacuum. 3 g of a crude containing 600 mg of compound 4were obtained.

I) Phosphoric anhydride (4.25 g; 30 mmol) was added portionwise, keepingthe temperature between 0° and 5° C., to a solution ofdimethylsulphoxide (2.34 g; 30 mmol), methylene chloride (21 ml),compound 3 (2.95 g; 10 mmol) and triethylamine (1 g; 10 mmol) cooled to0° C. The mixture was kept under stirring for 0.5 hours at 0° C. andthen triethylamine (3.6 g; 35 mmol) was added dropwise. After 1 hourfrom the end of the addition the reaction mixture was poured into water(50 ml). After separation of the phases the organic phase was dried oversodium sulphate and evaporated to residue under vacuum. 3 g of a crudecontaining 2.4 g of the compound 4 were obtained.

J) N-chlorosuccinimide (0.4 g; 3 mmol) was added portionwise to asolution of compound 3 (0.59 g; 2 mmol), dimethylsulphide (0.25 g; 4mmol) in methylene chloride (6 ml) cooled to -25° C. and kept undernitrogen. Triethylamine (0.3 g; 3 mmol) was added dropwise to thereaction mixture kept at -20° C. for 30 minutes. At the end of theaddition the mixture was heated to 0° C. and poured into water (10 ml).The phases were separated and the organic phase was dried over sodiumsulphate and evaporated to residue under vacuum. 0.6 g of a crudecontaining 4 were obtained.

K) 1-Oxo-2,2,6,6-tetramethylpiperidinium chloride, prepared according tothe method reported on J. Org. Chem., 53, 1278, (1988) (0.2 g; 1.04mmol), was added to a solution of compound 3 (0.148 g; 0.502 mmol) and2,6-lutidine (0.25 ml; 2.1 mmol) in methylene chloride (4 ml) keptbetween 0° and 5° C. The reaction mixture was kept between 0° and 5° C.under stirring for 30 minutes. The solution was then washed with 0.1Nhydrochloric acid, with a 5% sodium bicarbonate aqueous solution andthen with water; after separation of the phases the organic phase wasdried over sodium sulphate and evaporated to dryness under vacuum togive a residue (250 mg). The product was purified by columnchromatography (silica gel, eluent ethyl ether/ethyl acetate) to givethe pure 4 (0.11 g).

L) Molecular sieves 4A (8 g) were added to a solution of compound 3 (4.4g; 15 mmol) and N-methylmorfoline-N-oxide (3.0 g; 22.5 mmol) inmethylene chloride (50 ml) kept under stirring under nitrogen. After 10minutes tetrapropylammonium perruthenate (0.262 g; 0.75 mmol) was addedto the solution. The reaction mixture was kept at 25° C. for 2 hours.After separation of the molecular sieves by filtration, the reactionmixture was washed with 0.1N hydrochloric acid, with a 5% sodiumbicarbonate aqueous solution and with water and then dried over sodiumsulphate. By evaporation of the solvent under vacuum a residue (4.2 g)was obtained which after chromatography on silica gel (eluent ethylacetate) afforded the pure compound 4 (2.1 g; 7.2 mmol).

EXAMPLE 32

Preparation of compound 5 (see Example 4) from compound 4 (see Example3)

A) 1,4-Diazabicyclo-[2,2,2]-octane (300 mg; 2.66 mmol) was added at 45°C. under stirring to a solution of 4 (5 g; 16.9 mmol),n-propylpropionate (2 ml) and diisopropylether (6 ml). After 4 hours(ratio 5:4=60:40 as determined by HPLC of the solution) the solution wascooled to 40° C. and added with compound 5 (100 mg). The reactiontemperature was slowly cooled at 20° C. and kept at 20° C. for 15 hours.The suspension was then filtered and the solid was washed withdiisopropyl ether (2×2 ml).

After drying, 4 g of a mixture of 5 and 4 in ratio 97:3 were obtained.

Compound 4 (4.2 g) and n-propylpropionate (0.5 g) were added to asolution obtained by combining the filtrate and the isopropyl ethercoming from washings (4 ml). The mixture was kept at 40°-45° C. for 3hours, then cooled to 40° C. and added with compound 5 (100 mg). Thereaction mixture was then slowly cooled to 20° C. and kept understirring at 20° C. for 15 hours. The suspension was then filtered andthe solid was washed with diisopropylether (2×2 ml). 4.8 g of 5 and 4 inthe ratio 95:5 were obtained.

B) 1,4-Diazabicyclo-[2,2,2]-octane (300 mg; 2.66 mmol) was added at 45°C. under stirring to a solution of 4 (5 g; 16.9 mmol), isoamyl acetate(2 ml) and decahydronaphthalene (6 ml). After 4 hours (ratio 5:4=60:40as determined by HPLC in the solution) the solution was cooled to 40° C.and added with compound 5 (100 mg). The reaction temperature was slowlycooled to 20° C. and kept at 20° C. for 15 hours. The suspension wasthen filtered and the solid was washed with decahydronaphthalene (2×2ml).

After drying, 4 g of a mixture of 5 and 4 in the ratio 97:3 wereobtained.

Compound 4 (4.2 g) and isoamyl acetate (0.5 g) were added to a solutionobtained by the combining filtrate and the decahydronaphthalene washings(4 ml). The mixture was kept at 40°-45° C. for 3 hours, then cooled to40° C. and added with compound 5 (100 mg). The reaction mixture was thenslowly cooled to 20° C. and kept under stirring at 20° C. for 15 hours.The suspension was then filtered and the solid was washed withdecahydronaphthalene (2×2 ml). 4.8 g of 5 and 4 in the ratio 95:5 wereobtained.

C) 1,4-Diazabicyclo-[2,2,2]-octane (0.6 g; 0.0053 mol) was added to thecompound 4 (15 g; 0.5 mol) kept under stirring at 25° C. The reactionmixture was heated to 45° C. for 3 hours, then isoamyl acetate (9 ml)and diisopropylether (10 ml) were added and the mixture was left to coolspontaneously under stirring up to 25° C. After 1 hour isopropylether (5ml) was added and the mixture was cooled to 5° C. in 0.5 hours. It waskept at 5° C. for 0.5 hours. The suspension was filtered, washed withisopropylether (2×10 ml) to give 9.0 g of a solid formed by 5 and 4 inthe ratio 98:2.

D) 1,4-Diazabicyclooctane (2.5 g; 0.022 mol) was added to compound 4 (60g; 0.2 mol) kept under stirring at 25° C. Cyclohexane (120 ml) was addedto the reaction mixture heated to 50° C. for 2 hours; the reaction waskept at 50° C. for further 2 hours and then cooled to 25° C. After 16hours the reaction mixture was filtered; a mixture (55 g) of compounds 5and 4 in the ratio 94:6 was obtained.

E) 1,4-Diazabicyclo-[2,2,2]-octane (300 mg; 2.66 mmol) was added at 45°C. under stirring to a solution of compound 4 (5 g; 16.9 mmol) andpropylpropionate (2.5 ml) in methylcyclohexane (6 ml). After 5 hours,the solution was heated to 40° C. and added with compound 5 (100 mg) andwith propylpropionate (0.5 ml). The reaction temperature was slowlycooled to 20° C. and kept at 20° C. under stirring for 15 hours. Thesuspension was filtered and the solid was washed with methylcyclohexane(2×2 ml). The solid (3.5 g) formed by 5 and 4 in ratio 96:4 wasobtained.

EXAMPLE 33

Preparation of compound 6 (see Example 5) from compound 5 (see Example4)

Compound 5 (245 g; 0.83 mol) was added to a solution of boric acid (21.5g; 0.35 mol) in ethanol (2100 g). The solution was cooled to 0° C. andadded with sodium borohydride (13.2 g; 0.35 mol). The solution was keptunder stirring for 2 hours and then poured into a pH 7 buffered aqueoussolution and extracted with methylene chloride (2×500 g). The combinedorganic phases were washed with water and the solvent was evaporatedunder vacuum to give compound 6 (257 g).

EXAMPLE 34

Preparation of(4R,5S)-5-(4-methylthiophenyl)-4-acetoxymethyl-3-acetyl-2,2-dimethyl-1,3-oxazolidine(compound 26)

Acetyl chloride (3.2 g; 40.8 mmol) was added under stirring at 15° C. toa solution of compound 6 (see Example 5) (10 g; 33.9 mmol) andtriethylamine (4.2 g; 41.6 mmol) in methylene chloride (60 ml). After 1hour the reaction was poured into water (50 ml), after separation of thephases, the aqueous phase was extracted with methylene chloride (100 ml)and the combined organic phases were dried over sodium sulphate andevaporated under vacuum. The crude compound 26 was thus obtained whichwas directly used in the next step (Example 35).

EXAMPLE 35

Preparation of (2R,3R)-3-(4-methylthiophenyl)-2-amino-1,3-propanediol[(2R,3R)-Thiomicamine]

Compound 26 (see Example 34) (1.1 g; 3.30 mmol) was added at 35° C.under stirring and under nitrogen to a solution of methanesulphonic acid(0.36 g; 3.75 mmol) in methylene chloride (4 ml) and acetic anhydride(0.11 g; 1 mmol). After 30 hours the reaction mixture was added dropwiseto a sodium hydroxide solution (1.5 g; 37.5 mmol) in water (4 ml) keptat 20° C. At the end of the addition the mixture was heated to 95° C.for 4 hours. HPLC analysis of the aqueous solution showed the presenceof Thiomicamine (0.63 g; 2.97 mmol, 95% yield) with(2R,3R):(2R,3S)=89:11 diastereomeric ratio. The product, whichcrystallized by cooling the solution, was filtered at 5° C. and washedwith water (20 ml). After drying under vacuum the pure(2R,3R)-Thiomicamine (0.61 g; 2.88 mmol; 85% yield) was obtained.

EXAMPLE 36

Preparation of (2R,3R)-Thiomicamine from compound 6 (see Example 5)

A) Compound 6 (5.0 g; 16.9 mmol) was added at 15° C. under stirring andunder nitrogen to a solution of monohydrated p-toluenesulphonic acid(3.90 g; 20.5 mmol) in acetic anhydride (5.50 g; 53.9 mmol). Thereaction was then heated to 35° C. for 8 hours. At the end the solutionwas cooled to 15° C. and added dropwise to a sodium hydroxide solution(7.5 g; 187 mmol) in water (20 ml). The mixture was then heated to 95°C. for 4 hours under stirring and then cooled to 15° C. in 2 hours. Theprecipitate thus formed was filtered, washed with water (20 ml) anddried under vacuum at 60° C. to give pure (2R,3R)-Thiomicamine (3.07 g;14.4 mmol; 84.3% yield).

B) The experiment was carried out following the same procedure describedat point A but using monohydrated p-toluenesulphonic acid (0.78 g; 4.1mmol), acetic anhydride (1.05 g; 10.3 mmol), methylene chloride (4 ml)and compound 6 (1 g; 3.39 mmol). After treatment with sodium hydroxide(1.5 g of NaOH and 4 ml of water) according to the procedure describedat point A, Thiomicamine having the ratio (2R,3R):(2R,3S)=90:10 wasobtained.

C) The experiment was carried out following the same procedure describedat point A but using methanesulphonic acid (0.39 g; 4.1 mmol), aceticanhydride (0.64 g; 6.2 mmol), acetic acid (0.49 g; 8.2 mmol) andcompound 6 (1 g; 3.39 mmol). After treatment with sodium hydroxide (1.5g of NaOH and 4 ml of water) according to the procedure described atpoint A, Thiomicamine having the ratio (2R,3R):(2R,3S)=92.5:7.5 wasobtained.

D) The experiment was carried out following the same procedure describedat point A but using monohydrated p-toluenesulphonic acid (0.39 g; 2.05mmol), acetic anhydride (0.21 g; 2.0 mmol), formic acid (2 g) andcompound 6 (0.5 g; 1.69 mmol). After treatment with sodium hydroxide(1.5 g of NaOH and 4 ml of water) according to the procedure describedat point A, Thiomicamine having the ratio (2R,3R):(2R,3S)=88:12 wasobtained.

EXAMPLE 37

Preparation of (2R,3R)-Thiomicamine

By mild hydrolysis under controlled conditions of compound 6 (seeExample 5) (2R,3S)-3-(4-methylthiophenyl)-2-acetamido-1,3-propanediol(Compound 27) was obtained from which (2R,3R)-Thiomicamine was preparedaccording the following procedures:

A) Compound 27 (1.0 g; 3.92 mmol) was added at 15° C. under stirring andunder nitrogen to a solution of monohydrated p-toluenesulphonic acid(1.1 g; 5.78 mmol) in acetic anhydride (1.03 g; 9.98 mmol) and methylenechloride (8 ml). The reaction was heated to 25° C. for 16 hours. At theend the solution was cooled to 15° C. and added dropwise to a sodiumhydroxide solution (1.4 g; 35 mmol) in water (3 ml). The mixture wasthen heated to 95° C. for 5 hours. HPLC analysis of the aqueous solutionshowed the presence of Thiomicamine with diastereomeric ratio(2R,3R):(2R,3S)=84:16.

B) Compound 27 (1.0 g; 3.92 mmol) was added at 15° C. under stirring andunder nitrogen to a solution of monohydrated p-toluenesulphonic acid(1.1 g; 5.78 mmol) in acetic anhydride (1.1 g; 10.78 mmol) and aceticacid (8 ml). The reaction was kept at 25° C. for 35 hours.

The solvent was removed under vacuum at 40° C. and the residue was addedto a sodium hydroxide solution (1 g; 25 mmol) in water (4 ml). Themixture was then heated to 95° C. for 5 hours. HPLC analysis of theaqueous solution showed the presence of Thiomicamine with diastereomericratio (2R,3R):(2R,3S)=85:15.

EXAMPLE 38

Preparation of(4S,5S)-5-(4-methylthiophenyl)-4-hydroxymethyl-3-propionyl-2,2-dimethyl-1,3-oxazolidine(compound 28)

Propionyl chloride (2.2 g; 23.6 mmol) was added in 2 hours to a solutionof compound 7 (see Example 9) (5 g; 19.7 mmol) and triethylamine (2.4 g;23.6 mmol) in methylene chloride (70 ml) kept under stirring undernitrogen at 15° C. A 10% ammonium chloride aqueous solution (200 ml) wasthen added to the reaction mixture. After separation of the phases theaqueous phase was extracted with methylene chloride (100 ml).

The combined organic phases were dried over sodium sulphate andevaporated to dryness. A residue was obtained which aftercrystallization from ethyl acetate afforded the pure compound 28 (4.6 g;15 mmol, 77% yield) having the following characteristics:

¹ H-NMR (300 MHz, 80° C. in DMSO-d₆): δ(ppm): 0.99 (t, J=7.3 Hz, 3H),1.45 (s, 3H); 1.5 (s, 3H); 2.37 (q, J=7.3 Hz, 2H); 2.47 (s, 3H); 3.58(ddd, J=11.23 Hz, J=6.59 Hz, J=4.15 Hz, 1H); 4.08 (ddd, J=3.9 Hz, J=4.15Hz, J=6.59 Hz, 1H); 5.07 (d, J=3.9 Hz, 1H); 7.31 (AA'BB' system, Δν=42Hz, 4H).

EXAMPLE 39

Preparation of(4R,5S)-5-(4-methylthiophenyl)-4-formyl-3-propionyl-2,2-dimethyl-1,3-oxazolidine(compound 29)

A solution of dimethylsulphoxide (2.8 g; 3.6 mmol) in methylene chloride(5 ml) was added to a solution of oxalyl chloride (1.8 g; 14.1 mmol) inmethylene chloride (20 ml) kept at -60° C. under nitrogen. A solution ofcompound 28 (see Example 38) (4 g; 12.9 mmol) in methylene chloride (25ml) was added after 30 minutes to the solution.

Triethylamine (9.6 g; 92.9 mmol) was added under stirring to thereaction mixture kept at -60° C. for 30 minutes. The reaction mixturewas kept at -60° C. for 15 minutes, then it was heated to 0° C. in 1hour and poured into a 5% sodium bicarbonate solution (80 ml). Theaqueous phase was extracted with methylene chloride (30 ml); thecombined organic phases were dried over sodium sulphate and evaporatedunder vacuum to give an oily residue (Compound 29) (3.9 g) which wasused in the next step (Example 40).

EXAMPLE 40

Preparation of(4S,5S)-5-(4-methylthiophenyl)-4-formyl-3-propionyl-2,2-dimethyl-1,3-oxazolidine(compound 30)

1,4-Diazabicyclo-[2,2,2]-octane (0.13 g; 1.17 mmol) was added tocompound 29 (3.6 g; 11.7 mmol) (see Example 39) kept under mechanicalstirring at 40° C. under nitrogen.

The reaction was monitored by ¹ H-NMR (300 MHz); as soon as the ratio30:29 was equal to 40:60, crystals of compound 30 (10 mg) were added tothe reaction mixture.

At the end of the reaction (ratio 29:30=14:86) the suspension wasdissolved into a solution of acetic acid (0.071 g; 1.18 mmol) inmethylene chloride (10 ml). The organic phase was washed with water,dried over sodium sulphate and evaporated under vacuum. A residue (3.5g) was obtained which was crystallized from isopropanol/isopropyl etherat -10° C. to give pure compound 30 formed by two rotamers (¹ H-NMR inCDCl₃):

Major rotamer ¹ H-NMR (CDCl₃): δ(ppm): 1.08 (part X of an ABX₃ system,J=7.3 Hz); 1.73 (s, 3H); 1.86 (s, 3H); 1.99 (part A of an ABX₃ system,J=7.3 Hz, J=16 Hz, 2H); 2.16 (part B of an ABX₃ system, J=7.3 Hz, J=16Hz, 2H); 2.48 (s, 3H); 4.49 (dd, J=2.8 Hz, J=6.4 Hz, 1H); 5.44 (d, J=6.4Hz, 1H); 7.26 (AA'BB' system, Δν=22 Hz, 4H); 9.17 (d, J=2.9 Hz, 1H).

Minor rotamer ¹ H-NMR (CDCl₃): δ(ppm): 1.2 (t, 3H, J=7.3 Hz); 1.6 (s,3H); 1.89 (s, 3H); 2.1 (m, Δν=60 Hz, 2H); 2.47 (s, 3H); 5.01 (d, J=7.1Hz, 1H); 5.36 (d, J=7.1 Hz, 1H); 7.27 (AA'BB' system, Δν=22 Hz, 4H);9.06 (s, 1H).

EXAMPLE 41

Preparation ofthreo-(2R,3S)-3-hydroxy-3-(4-methylthiophenyl)-2-acetamido propionicacid methyl ester (Compound 31)

A solution of (2R,3S)-3-hydroxy-3-(4-methylthiophenyl)-2-acetamidopropionic acid (1.5 g; 5.5 mmol) (prepared according to the proceduredescribed in Italian Patent No. 1,196,434), anhydrous p-toluenesulphonicacid (0.032 g; 0.18 mmol) and trimethylorthoformate (0.18 g; 1.68 mmol)in methyl alcohol (15 ml) was stirred under nitrogen at 25° C. for 16hours.

The reaction mixture was filtered to give compound 31 (solid A), whilethe mother liquors were evaporated under vacuum to give a residue (1.2g). A 5% sodium bicarbonate aqueous solution (5 ml) was added to theresidue and the mixture was stirred for 10 minutes. The heterogeneousmixture was filtered, the insoluble (solid B) was washed with water (5ml) and then with acetone (5 ml). The combined solids (A and B) (0.8 g;2.82 mmol; 51% yield) were crystallized from ethyl alcohol to give purecompound 31.

[α]_(D) ²⁵ =-14.7° (c 0.17, CHCl₃) m.p.=189°-191° C. I.R. (KBr): 3361cm⁻¹, 1756 cm⁻¹, 1650 cm⁻¹, 1530 cm⁻¹. ¹ H-NMR (300 MHz, CDCl₃ +D₂ O):δ(ppm): 1.96 (s, 3H); 2.48 (s, 3H); 3.76 (s, 3H); 4.85 (dd, J=8.7 Hz,J=3.2 Hz, 1H); 5.23 (d, J=3.2 Hz, 1H); 6.23 (d, J=8.7 Hz, 1H); 7.21-7.29(aromatic protons, 4H).

EXAMPLE 42

Preparation of(4R,5S)-5-(4-methylthiophenyl)-4-(methoxycarbonyl)-3-acetyl-2,2-dimethyl-1,3-oxazolidine(Compound 32)

2,2-Dimethoxypropane (21.6 g; 207 mmol) and anhydrous p-toluenesulphonicacid (0.087 g; 0.5 mmol) were added to a vigorously stirred mixture ofcompound 31 (2.5 g; 8 mmol) and acetone (5 ml) at 25° C. and undernitrogen.

The mixture was heated at 65° C. for 2.5 hours, cooled to 25° C., andpoured into a mixture of 5% NaHCO₃ aqueous solution (40 ml) andmethylene chloride (50 ml). The mixture was stirred at 25° C. for 10minutes. The organic layer was separated, dried over Na₂ SO₄ andevaporated under reduced pressure to give crude compound 32 (1.94 g).The crude product was purified by chromatography (silica gel, eluentethylacetate) affording pure compound 32, which consists, on the base of¹ H-NMR data, of two rotamers (restricted rotation of the amido group)in ratio 60:40. I.R. (CCl₄): 1756 cm⁻¹, 1672 cm⁻¹, 1390 cm⁻¹.

Major rotamer (60%) ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.69 (s, 3H); 1.78(s, 3H); 1.91 (s, 3H); 2.49 (s, 3H); 3.81 (s, 3H); 4.35 (d, J=6.8 Hz,1H); 5.10 (d, J=6.8 Hz, 1H); 7.25-7.33 (aromatic protons, 4H).

Minor rotamer (40%) ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.78 (s, 3H); 2.19(s, 3H); 2.48 (s, 3H); 3.74 (s, 3H); 4.41 (d, J=8.3 Hz, 1H); 5.01 (d,J=8.3 Hz, 1H); 7.15-7.25 (aromatic protons, 4H).

EXAMPLE 43

Preparation of(4S,5S)-5-(4-methylthiophenyl)-4-(methoxycarbonyl)-3-acetyl-2,2-dimethyl-1,3-oxazolidine(Compound 33)

Sodium methoxide (0.37 g; 6.8 mmol) was added to a solution of crudecompound 32 (2 g) in methyl alcohol (10 ml); the reaction mixture wasstirred at 40° C. under nitrogen for 72 hours. The reaction mixture wascooled to 25° C. and added under stirring with a mixture of 0.1N HCl (20) and methylene chloride (30 ml).

The organic layer was separated and dried over Na₂ SO₄ and evaporatedunder reduced pressure to give an oily residue (1.1 g) consisting of amixture of compound 32 and compound 33 in 32:33=40:60 ratio (¹ H-NMR).

Analytically pure compound 33, obtained by flash column chromatography(silica gel, eluent diethylether), was, on the base of ¹ H-NMR spectrain CDCl₃, a mixture of two rotamers due to restricted rotation of theamido group. I.R. (CCl₄): 1758 cm⁻¹, 1672 cm⁻¹, 1398 cm⁻¹.

Major rotamer (82%) ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.70 (s, 3H); 1.92(s, 3H); 1.97 (s, 3H); 2.48 (s, 3H); 3.29 (s, 3H); 4.57 (d, J=6.6 Hz,1H); 5.40 (d, J=6.6 Hz, 1H); 7.21-7.30 (aromatic protons, 4H).

Minor rotamer (18%) ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.72 (s, 3H); 1.96(s, 3H); 2.22 (s, 3H); 2.48 (s, 3H); 3.23 (s, 3H); 4.83 (d, J=6.6 Hz,1H); 5.31 (d, J=6.6 Hz, 1H); 7.21-7.30 (aromatic protons, 4H).

EXAMPLE 44

Preparation of(4S,5S)-3-acetyl-2,2-dimethyl-4-hydroxymethyl-5-phenyl-1,3-oxazolidine(Compound 34)

A stirred mixture of enantiomerically pure(+)-(1S,2S)-2-amino-1-phenyl-1,3-propanediol (200 g; 1.19 mol), toluene(700 ml) and acetone (440 ml; 6 mol) was heated at reflux for 12 hoursbeneath a Dean Stark trap: a mixture of toluene, water and acetone wascollected. The solvent was distilled under vacuum (internal temperature80° C.) to give a residue (210 g).

Acetylchloride (82.5 g; 1.07 mol) was added in 1 hour at 0° C. to astirred solution of the residue (200 g; 0.965 mol) and of triethylamine(108 g; 1.07 mol) in methylene chloride (800 ml). The reaction mixturewas stirred for 3 hours at 15° C., then it was poured into water (300ml). The organic phase was separated and the aqueous phase was extractedwith methylene chloride (600 ml): the combined organic extracts werewashed with 0.1N hydrochloric acid (300 ml) and then with water (300ml), dried over sodium sulphate and concentrated under vacuum to give aresidue (240 g), which, after crystallization from diethyl ether gavepure compound 34 (140 g; 0.57 mol; 59% yield).

Major rotamer: ¹ H-NMR (300 MHz, DMSO+D₂ O): δ(ppm): 1.46 (s, 3H); 1.49(s, 3H); 2.05 (s, 3H); 3.56 (dd, J=11.48 Hz, J=4.0 Hz, 1H); 3.64 (dd,J=11.48 Hz, J=6.84 Hz, 1H); 4.08 (ddd, J=6.84 Hz, J=4.0 Hz, J=3.9 Hz,1H); 5.09 (d, J=3.9 Hz, 1H); 7.30-7.46 (aromatic protons, 5H).

Minor rotamer: ¹ H-NMR (300 MHz, DMSO+D₂ O): δ(ppm): 1.58 (s, 3H); 1.65(s, 3H); 2.05 (s, 3H); 3.82 (broad signal, 2H); 4.23 (broad signal, 1H);5.09 (broad signal, 1H); 7.30-7.46 (aromatic protons, 5H).

EXAMPLE 45

Preparation of(4R,5S)-5-phenyl-4-formyl-3-acetyl-2,2-dimethyl-1,3-oxazolidine(Compound 35)

A mixture of(4S,5S)-5-phenyl-4-hydroxymethyl-3-acetyl-2,2-dimethyl-1,3-oxazolidine(5 g; 20 mmol), methylene chloride (20 ml),2,2,6,6-tetramethylpiperidinyl-1-oxy (TEMPO) (0.031 g; 0.2 mmol),potassium bromide (0.195 g; 2 mmol) and water (2 ml) was cooled to 0° C.(water-ice bath). The mixture, under vigorous stirring, was addeddropwise in 30 minutes to a solution prepared by adding a 5% sodiumbicarbonate aqueous solution and then 1N HCl to sodium hypochlorite(23.1 ml; 24.9 mmol) (the pH of the solution was 8.7). The mixture wasstirred for 30 minutes at 0° C. and the reaction was followed by TLC(silica gel, ethyl acetate as eluent). The phases were separated, theaqueous phase was extracted with methylene chloride (3×10 ml), thecombined organic extracts were washed with a 5% sodium bicarbonateaqueous solution (10 ml) and with water (10 ml). The organic phase wasdried over sodium sulphate. Evaporation of the solvent under reducedpressure gave the oily aldehyde 35 (4.65 g; 18.8 mmol; 94% yield) which,on the base of ¹ H-NMR data, in chloroform, consists of two rotamers(restricted rotation of the amido group) in ratio 53:47.

I.R. (CCl₄): 1740 cm⁻¹, 1672 cm⁻¹, 1390 cm⁻¹.

Major rotamer (53%): ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.69 (s, 3H);1.81 (s, 3H); 2.22 (s, 3H); 4.48 (dd, J=8.8 Hz, J=2.7 Hz, 1H); 5.02 (d,J=8.8 Hz, 1H); 7.35-7.45 (aromatic protons, 5H); 9.60 (d, J=2.7 Hz, 1H).

Minor rotamer (47%): ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.77 (s, 3H);1.81 (s, 3H); 1.94 (s, 3H); 4.34 (dd, J=6.9 Hz, J=3.1 Hz, 1H); 5.14 (d,J=6.9 Hz, 1H); 7.35-7.45 (aromatic protons, 5H); 9.68 (d, J=3.1 Hz, 1H).

EXAMPLE 46

Preparation of(4S,5S)-5-phenyl-4-formyl-3-acetyl-2,2-dimethyl-1,3-oxazolidine(Compound 36)

An homogeneous mixture of 1,4-diazabicyclo-[2,2,2]-octane (DABCO) (0.197g; 1.76 mmol) and compound 35 (4.36 g; 17.6 mmol) was stirred at 40° C.for 3 hours; the reaction mixture was kept under stirring for additional2 hours at 15° C. [35:36=40:60 as determined after acidic removal DABCO(see below) by ¹ H-NMR in CDCl₃ on the base of integrals of thealdehydic protons].

The reaction mixture was poured into a vigorously stirred mixture ofmethylene chloride (30 ml) and of a solution prepared by diluting up to15 ml 0.5N hydrochloric acid (3.6 ml).

The aqueous phase was extracted with methylene chloride (15 ml). Thecombined organic extracts were dried over sodium sulphate and evaporatedunder vacuum.

The residue (4.3 g) consisted of a mixture of compounds 35 and 36 in35:36=40:60 ratio as determined by ¹ H-NMR analysis in CDCl₃ on the baseof integrals of aldehydic protons.

Compound 36

Major rotamer: ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.75 (s, 3H); 1.87 (s,3H); 1.94 (s, 3H); 4.52 (dd, J=6.4 Hz, J=2.7 Hz, 1H); 5.51 (d, J=6.4 Hz,1H); 7.35-7.45 (aromatic protons, 5H); 9.15 (d, J=2.7 Hz, 1H).

Minor rotamer: ¹ H-NMR (300 MHz, CDCl₃): δ (ppm): 1.65 (s, 3H); 1.91 (s,3H); 2.24 (s, 3H); 5.05 (broad d, J=7.0 Hz, 1H); 5.41 (d, J=7.0 Hz, 1H);7.3-7.5 (aromatic protons, 5H); 9.03 (broad s, 1H).

EXAMPLE 47

Preparation of(4R,5R)-5-(4-methylthiophenyl)-4-acetoxymethyl-2-methyl-1,3-oxazoline asp-toluenesulphonic salt (Compound 37) and of(2R,3R)-3-(4-methylthiophenyl)-2-amino-1,3-propanediol[(2R,3R)-thiomicamine]

Anhydrous p-toluenesulphonic acid (3.9 g; 22.7 mmol) was added dropwiseat 25° C. to a stirred solution of acetic anhydride (3.35 g; 32.8 mmol),acetic acid (1 g; 16.6 mmol) and(4R,5S)-5-(4-methylthiophenyl)-4-hydroxymethyl-3-acetyl-2,2-dimethyl-1,3-oxazolidine(Compound 6) (5 g; 16.9 mmol).

The reaction mixture was then heated to 35° C. and kept at thistemperature for 4 hours. Removal of acetone under vacuum and cooling to15° C. gave a solution of(4R,5R)-5-(4-methylthiophenyl)-4-acetoxymethyl-2-methyl-1,3-oxazoline asp-toluenesulphonic salt (compound 37) and of p-toluenesulphonic acid,acetone and acetic acid.

¹ H-NMR (300 MHz, CDCl₃): δ (ppm): 2.17 (s, 3H); 2.47 (s, 3H); 2.61 (s,3H); 4.42 (dd, J=5.3 Hz, J=12.1 Hz, 1H); 4.46 (dd, J=4.3 Hz, J=12.1 Hz,1H); 4.80 (ddd, J=5.3 Hz, J=4.3 Hz, J=8.1 Hz, 1H); 5.79 (d, J=8.1 Hz,1H); 7.22-7.35 (aromatic protons, 4H); 7.18-7.67 (aromatic protons, 4H).

The crude product was slowly added at 15° C. to a solution of sodiumhydroxide (5 g) in water (20 ml) and the reaction mixture was thenheated to 98° C. and kept at 98° C. for 4.5 hours.

Cooling the solution to 15° C. in 2 hours caused the precipitation of(2R,3R)-thiomicamine which was filtered, washed with water and driedunder vacuum at 60° C. Pure (2R,3R)-thiomicamine was obtained (3.05 g;81% yield) [α]_(D) ²⁰ =-33.8° (c 2, 0.2N HCl)

EXAMPLE 48

Preparation of(4R,5S)-5-(4-methylthiophenyl)-3-acetyl-4-acetoxymethyl-2,2-dimethyl-1,3-oxazolidine(Compound 26)

Acetylchloride (3.2 g, 40.8 mmol) was added in 1 hour at 25° C. to astirred solution of compound 6 (10 g; 33.9 mmol) and of triethylamine(4.2 g; 41.6 mmol) in methylene chloride (60 ml). The reaction mixturewas stirred for 2 hours at 25° C., then it was poured into water (50ml). The organic phase was separated and the aqueous phase was extractedwith methylene chloride (100 ml): the combined organic extracts werewashed with water (50 ml), dried over sodium sulphate and concentratedunder vacuum to give a residue (11.4 g), which was purified bychromatography on silica gel (eluent: ethyl acetate/hexane=1:1) to givepure compound 26 (10.2 g; 30.2 mmol; 89% yield).

¹ H-NMR (300 MHz, DMSO): δ (ppm): 1.60 (s, 3H); 1.62 (s, 3H); 1.73 (s,3H); 2.10 (s, 3H); 2.47 (s, 3H); 3.70 (dd, J=5.67 Hz, J=11.63 Hz, 1H);3.78 (dd, J=6.64 Hz, J=11.63 Hz, 1H); 4.53 (ddd, J=5.12 Hz, J=6.64 Hz,J=5.67 Hz, 1H); 5.35 (d, J=5.12 Hz, 1H); 7.22-7.36 (aromatic protons,4H).

EXAMPLE 49

Preparation of(4S,5S)-5-(4-methylsulphonylphenyl)-3-acetyl-4-hydroxymethyl-2,2-dimethyl-1,3-oxazolidine(Compound 38)

A solution of 42% hydrogen peroxyde (2.5 ml; 30 mmol) was added in 1hour, under stirring at 50° C., to a solution of compound 3 (2.95 g; 10mmol), sodium tungstate dihydrate (11 mg) and EDTA (5 mg) in methanol (5ml). The mixture was kept at 50° C. for 1 hour. After evaporation of thesolvent under vacuum, the residue was treated with a mixture ofmethylene chloride (30 ml) and water (30 ml). The phases were separatedand the organic phase was dried over sodium sulphate and evaporatedunder vacuum to give crude compound 38 (2.8 g).

Major rotamer: ¹ H-NMR (300 MHz, CDCl₃ +D₂ O): δ (ppm): 1.78 (s, 3H);2.23 (s, 3H); 3.05 (s, 3H); 3.72 (dd, J=5.64 Hz, J=12.0 Hz, 1H); 3.84(dd, J=12.0 Hz, J=3.23 Hz, 1H); 4.03 (ddd, J=8.62 Hz, J=5.64 Hz, J=3.23Hz, 1H); 4.82 (d, J=8.60 Hz, 1H); 7.60-7.80 (aromatic protons, 4H).

Minor rotamer: ¹ H-NMR (300 MHz, CDCl₃ +D₂ O): δ (ppm): 1.68 (s, 3H);2.11 (s, 3H); 3.05 (s, 3H); 3.84 (m, 2H); 4.03 (m, 1H); 5.31 (d, J=3.71Hz, 1H); 7.60-7.80 (aromatic protons, 4H).

EXAMPLE 50

Preparation of(4R,5S)-5-(4-methylsulphonylphenyl)-3-acetyl-4-formyl-2,2-dimethyl-1,3-oxazolidine(Compound 39)

A solution of m-chloroperbenzoic acid (assay 75%, 24.5 g; 115 mmol) inmethylene chloride (25 ml) was added in 1 hour, under stirring at 25°C., to a solution of compound 4 (15.3 g; 52.3 mmol), in methylenechloride (190 ml). The mixture was kept at 25° C. for 2 hours, thenpoured in 5% sodium bicarbonate aqueous solution (100 ml). Afterseparation of the phases, the organic phase was washed with water (50ml), dried over sodium sulphate and evaporated under vacuum to givecrude compound 39 (10.5 g; 32.4 mmol; 62% yield).

Major rotamer ¹ H-NMR (300 MHz, CDCl₃): δ (ppm): 1.78 (s, 3H); 1.83 (s,3H); 2.25 (s, 3H); 3.07 (s, 3H); 4.40 (dd, J=2.39, J=8.49, 1H); 5.11 (d,J=8.49, 1H); 9.61 (d, J=2.39, 1H); 7.55-8.05 (aromatic protons, 4H).

Minor rotamer ¹ H-NMR (300 MHz, CDCl₃): δ (ppm): 1.71 (s, 3H); 1.83 (s,3H); 2.25 (s, 3H); 3.07 (s, 3H); 4.28 (dd, J=2.74, J=6.73, 1H); 5.24 (d,J=6.73, 1H); 9.73 (d, J=2.74, 1H); 7.55-8.05 (aromatic protons, 4H).

EXAMPLE 51

Preparation of(4S,5S)-5-(4-methylsulphonylphenyl)-3-acetyl-4-formyl-2,2-dimethyl-1,3-oxazolidine(Compound 40)

1,4-Diazabicyclo-[2,2,2]-octane (35 mg; 0.3 mmol) was added understirring at 40° C. to a solution of compound 39 (1 g; 3 mmol) in toluene(0.5 ml). After 20 hours a diastereomeric ratio 40:39=48:52 was reached(as determined via ¹ H-NMR on the solution).

EXAMPLE 52

Preparation of(4S,5S)-5-(4-methylsulphonylphenyl)-3-acetyl-4-formyl-2,2-dimethyl-1,3-oxazolidine(Compound 40)

A solution of m-chloroperbenzoic acid (assay 3.2 g; 15 mmol) inmethylene chloride (15 ml) was added in 1 hour, under stirring at 25°C., to a solution of compound 5 (2 g; 6.8 mmol), in methylene chloride(15 ml). The mixture was kept at 25° C. for 2 hours, then poured in 5%sodium bicarbonate aqueous solution (15 ml). After separation of thephases, the organic phase was washed with water (15 ml), dried oversodium sulphate and evaporated under vacuum to give crude compound 40(1.8 g; 90% yield). Pure compound 40 was obtained by chromatography onsilica gel (eluent: ethyl acetate).

Major rotamer: ¹ H-NMR (300 MHz, CDCl₃): δ (ppm): 1.76 (s, 3H); 1.87 (s,3H); 1.96 (s, 3H); 3.07 (s, 3H); 4.59 (dd, J=6.21 Hz, J=3.04 Hz, 1H);5.58 (d, J=6.21 Hz, 1H); 7.60-8.10 (aromatic protons, 4H); 9.16 (d,J=3.04 Hz, 1H).

Minor rotamer: ¹ H-NMR (300 MHz, CDCl₃): δ (ppm): 1.66 (s, 3H); 1.87 (s,3H); 1.93 (s, 3H); 3.09 (s, 3H); 5.08 (dd, J=7.08 Hz, J=1.60 Hz, 1H);5.49 (d, J=7.08 Hz, 1H); 7.60-8.10 (aromatic protons, 4H); 9.05 (d,J=1.60 Hz, 1H).

EXAMPLE 53

Preparation of enantiomerically pure (+)-(2S,3S)-Thiomicamine

Enantiomerically pure (+)-thiomicamine was obtained in 90% yield bycrystallization of crude (+)-thiomicamine (50 g; e.e. 90%) fromisopropanol (1000 ml).

[α]_(D) ²⁰ =+33.2° (c 2, 0.1N HCl)-m.p. 151°-152° C. ¹ H-NMR (300 MHz,DMSO-D₂ O): δ (ppm): 2.43 (s, 3H); 2.64 (ddd, J=6.35, J=6.10, J=4.88,1H); 3.09 (dd, J=10.50, J=6.35, 1H); 3.38 (dd, J=10.50, J=4.88, 1H);4.37 (d, J=6.1, 1H); 7.21 (4H, aromatics). ¹³ C-NMR (DMSO-D₂ O): 15.01,59.00, 63.08, 72.76, 125.70, 127.17, 136.02, 141.07.

EXAMPLE 54

(4S,5S)-5-(4-methylthiophenyl)-4-hydroxymethyl-3-acetyl-2,2-dimethyl-1,3-oxazolidine(Compound 3)

A stirred mixture of enantiomerically pure (+)-thiomicamine (100 g;0.469 mol), toluene (920 ml) and acetone (100 ml) was heated at refluxfor 18 hours beneath a Dean Stark trap: a mixture of toluene, water andacetone (11 g) was collected. The solvent (200 ml) was distilled atambient pressure and then under vacuum (internal temperature 80° C.) togive compound 7 (118.6 g) as residue.

¹ H-NMR (300 MHz, DMSO): δ (ppm): 1.47 (s, 3H); 1.50 (s, 3H); 2.47 (s,3H); 3.09 (ddd, J=5.67, 4.17 and 11.4, 1H); 3.70 (ddd, J=5.67, 6.64 and11.4, 1H); 4.06 (ddd, J=3.84, 6.64 and 4.17, 1H); 5.06 (d, J=3.84, 1H);5.24 (t, J=5.67, 1H); 7.21-7.27 (aromatic protons, 4H).

Acetylchloride (38.3 g; 0.49 mol) was added in 1 hour at 15° C. to astirred solution of crude compound 7 and of triethylamine (70.6 g; 0.7mol) in methylene chloride (1170 ml). The reaction mixture was stirredfor 12 hours at 15° C., then it was poured into 0.5N hydrochloric acid(750 ml). The organic phase was separated and the aqueous phase wasextracted with methylene chloride (300 ml): the combined organicextracts were washed with water (300 ml), dried over sodium sulphate andconcentrated under vacuum to give a residue (120 g) which, aftercrystallization from methanol (140 ml), gave pure compound 3 (67.8 g;0.23 mol; 49% yield).

¹ H-NMR (300 MHz, DMSO): δ (ppm): 1.47 (s, 3H); 1.50 (s, 3H); 2.06 (s,3H); 2.47 (s, 3H); 3.55 (ddd, J=5.7, 11.5 and 4.0, 1H); 3.61 (ddd,J=5.7, 11.5 and 6.8, 1H); 4.06 (ddd, J=3.8, 4.0 and 6.8, 1H); 5.07 (d,J=3.8, 1H); 5.24 (t, J=5.7, 1H); 7.27-7.41 (aromatic protons, 4H). ¹³C-NMR (DMSO): 166.7; 137.7; 137.2; 127.2; 125.8; 95.2; 78.3; 64.6; 61.1;26.8; 26.24; 23.5; 14.6. [α]_(D) ²⁰ =+16.9° (c 1.0, CHCl₃) I.R. (KBr):3280, 1630 cm⁻¹. M.p.=142°-145° C. MS: m/e (rel. intensity): 296 M+1;100), 280 (11), 238 (39).

EXAMPLE 55

Preparation of(4R,5S)-5-(4-methylthiophenyl)-4-formyl-3-acetyl-2,2-dimethyl-1,3-oxazolidine(Compound 4)

A solution of dimethylsulphoxide (40.3 g; 0.51 mol) in methylenechloride (100 ml) was added in 30 minutes at -60° C. under nitrogen to astirred solution of oxalyl chloride (26.2 g; 0.21 mol) in methylenechloride (100 ml). The solution was stirred at -60° C. for 30 minutes. Asolution of compound 3 (50.9 g; 0.17 mol) in methylene chloride (600 ml)was added dropwise in 30 minutes at -60° C. to the previously preparedsolution. The reaction mixture was kept under stirring at -60° C. for 15minutes and then warmed up to -50° C. Triethylamine (91.0 g; 0.96 mol)was added under stirring in 20 minutes to the solution kept at -50° C.The reaction mixture was allowed to warm up to 0° C. in 2 hours and thenit was poured into a 10% ammonium chloride aqueous solution (300 ml).The organic phase was separated and aqueous phase was extracted withmethylene chloride (200 ml); the combined organic extracts were washedwith water (200 ml), dried over sodium sulphate and the solvent wasevaporated under vacuum to give oily crude compound 4 (51.5 g) (HPLCassay >95% determined as compound 3 after reduction with sodiumborohydride, yield ≧95%), which consisted, on the basis of the ¹ H-NMRdata, of two rotamers in ratio 56:44.

Major rotamer: ¹ H-NMR (300 MHz, CDCl₃): δ (ppm): 1.74 (s, 3H); 1.70 (s,3H); 2.16 (s, 3H); 2.42 (s, 3H); 4.35 (dd, J=8.79 and 2.91, 1H); 4.91(d, J=8.79, 1H); 7.19-7.24 (aromatic protons, 4H); 9.50 (d, J=2.91, 1H).

Minor rotamer: ¹ H-NMR (300 MHz, CDCl₃): δ (ppm): 1.62 (s, 3H); 1.74 (s,3H); 1.88 (s, 3H); 2.43 (s, 3H); 4.28 (dd, J=6.83 and 2.93, 1H); 5.06(d, J=6.83, 1H); 7.27-7.30 (aromatic protons, 4H); 9.61 (d, J=2.93, 1H).

Rotamers mixture: ¹³ C-NMR (74.5 MHz, CDCl₃): δ (ppm): 15.45; 21.59;24.12; 24.54; 26.17; 26.32; 28.08; 71.10; 72.42; 75.20; 76.16; 93.94;97.58; 126.85; 126.67; 126.54; 133.55; 132.78; 139.56; 139.77; 167.17;195.64; 196.56. I.R. (CCl₄): 2980, 1742, 1732, 1673 cm⁻¹. MS: m/e(rel.intensity): 294 (M+1; 78), 236 (100).

EXAMPLE 56

Preparation of(4S,5S)-5-(4-methylthiophenyl)-4-formyl-3-acetyl-2,2-dimethyl-1,3-oxazolidine(Compound 5)

An homogeneous mixture of 1,4-diazabicyclo-[2,2,2]-octane (1.44 g; 12.8mmol) and the crude product 4 (51.5 g) was stirred at 40° C. Themixture, which became heterogeneous (after 3 hours compound 5 started tocrystallize from the reaction mixture), was cooled to 35° C. and thenstirred for 2 hours at 35° C. The almost solid mixture was cooled to 25°C. and kept at 25° C. for 3 hours [4:5=5:95 as determined after acidicremoval of DABCO (see below) by ¹ H-NMR in CDCl₃ on the base ofintegrals of aldehydic protons]. The reaction mixture was poured into avigorously stirred mixture of methylene chloride (150 ml) and of asolution prepared by diluting up to 100 ml 0.5N hydrochloric acid (26ml). The aqueous phase was extracted with methylene chloride (150 ml).The combined organic extracts were dried over sodium sulphate andevaporated under vacuum. The residue (51 g) consisted of a mixture of 4and 5 in the ratio 4:5=5:95 as determined by ¹ H-NMR. The residue wascrystallized from 4-t-butyltoluene (100 ml) affording pure 5 (38.5 g;0.13 mol; 76% yield calculated on compound 3).

Major rotamer: ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.73 (s, 3H); 1.93 (s,3H); 2.48 (s, 3H); 4.49 (dd, J=2.8 and 6.4, 1H); 5.46 (d, J=6.4, 1H);7.23-7.31 (aromatic protons, 4H); 9.17 (d, J=2.8, 1H).

Minor rotamer: ¹ H-NMR (300 MHz, CDCl₃): δ(ppm): 1.64 (s, 3H); 1.89 (s,3H); 2.23 (s, 3H); 2.47 (s, 3H); 5.00 (dd, J=7.0, 1H); 5.36 (d, J=7.0,1H); 7.23-7.31 (aromatic protons, 4H); 9.06 (s broad, 1H).

Major rotamer: ¹³ C-NMR (74.5 MHz, CDCl₃): δ(ppm): 15.26; 23.67; 25.92;69.22; 77.06; 95.99; 126.39; 129.44; 139.54; 164.41; 196.58. [α]_(D) ²⁰=+124.3° (c 1, CHCl₃) M.p.=97°-102° C. I.R. (KBr): 1735, 1660, 1645 cm⁻¹MS m/e (rel.intensity): 294 (M+1; 100), 236 (35), 153 (20).

EXAMPLE 57

DABCO catalyzed epimerization of compound 4 (or 5) in toluene

A solution of 4 (2.95 g; 10.04 mmol), 1,4-diazabicyclo-[2,2,2]-octane(44.9 mg; 0.4 mmol) in toluene (29.5 ml) was stirred at 60° C. for 24hours. ¹ H-NMR analysis of the solution [4-methylthiobenzaldehyde (380mg; 2.5 mmol; internal standard)] showed the present of 4 and 5 in ratio45:55, [(4+5) accounts for 94% of the starting 4]. The same result wasobtained starting from 5.

EXAMPLE 58

Preparation of compound 6

Sodium borohydride (4.9 g; 0.13 mol) was added at 5° C. to a stirredmixture of calcium chloride (14.3 g; 0.13 mol) and of a solution of 5(53.7 g; 0.18 mol) and of tetrahydrofuran (220 ml) in ethanol (570 ml).The mixture was stirred for 2 hours at 5° C. and then poured into amixture of pH 7.00 aqueous solution (300 ml, 0.05M K₂ HPO₄ adjusted topH 7.00 with H₃ PO₄) and methylene chloride (400 ml). The aqueous phasewas extracted with methylene chloride (300 ml), the combined organicextracts were dried over sodium sulphate and the solvent evaporatedunder vacuum to give the crude compound 6 (54.7 g; HPLC assay 96%, yield97%). Analytically pure 6 was obtained by crystallization of the crude 6from toluene.

¹ H-NMR (300 MHz, DMSO): δ(ppm): 1.58 (s, 3H); 1.62 (s, 3H); 2.10 (s,3H); 2.46 (s, 3H); 3.03 (ddd, J=11.2, 5.1 and 5.3, 1H); 3.18 (ddd,J=11.2, 8.0 and 5.3, 1H); 4.25 (ddd, J=5.0, 8.0 and 5.1, 1H); 4.65 (t,J=5.3, 1H); 5.25 (d, J=5.0, 1H); 7.22-7.32 (aromatic protons, 4H). ¹³C-NMR (74.5 MHz, DMSO): δ(ppm): q 14.66; q 23.65; q 24.07; q 27.01; t60.65; d 61.85; d 76.34; d 93.33; d 125.55; d 126.65; s132.44; s 137.22;s 167.70. [α]_(D) ²⁰ =+80.8° (c 1.0, CHCl₃) I.R. (KBr): 3320, 1630 cm⁻¹.M.p.=123° -128° C. MS: m/e (rel.intensity): 296.1 (M+1; 100), 238.1(60), 220 (11).

EXAMPLE 59

Preparation of enantiomerically pure(+)-(2R,3S)-2-amino-3-(methylthiophenyl)-1,3-propanediol[(2R,3S)-Thiomicamine]

Sodium hydroxide (1.76 g; 44 mmol) was added at room temperature to asuspension of crude 6 (10 g; 33.9 mmol) in water (17 ml); the suspensionwas heated at reflux for 8 hours. The solution was added with water (25ml) and cooled in 1 hour to 15° C. The heterogeneous mixture wasfiltered, the insoluble washed with water (15 ml) and dried under vacuumto give crude (2R,3S)-thiomicamine (6.65 g). Crystallization fromtoluene gave the enantiomerically pure compound (6.0 g; 83% yield).

¹ H-NMR (300 MHz, DMSO-D₂ O): δ(ppm): 2.45 (s, 3H); 2.78 (ddd, J=7.00,J=6.23, J=4.54, 1H); 3.26 (dd, J=10.44, J=7.00, 1H); 3.38 (dd, J=10.44,J=4.54, 1H); 4.37 (d, J=6.23, 1H); 7.23-7.28 (4H, aromatics). ¹³ C-NMR(74.5 MHz, DMSO-D₂ O): δ(ppm): 14.96; 58.24; 63.03; 74.16; 125.60;127.56; 136.12; 140.28. [α]_(D) ²⁰ =-32.8° (c 2, HCl 0.1N)M.p.=117°-119° C.

EXAMPLE 60

Preparation of(-)-(2R,3R)-3-(4-methylthiophenyl)-2-amino-1,3-propanediol[(2R,3R)-Thiomicamine]

p-Toluenesulphonic acid monohydrated (20 g; 105 mmol) was added at 25°C. under stirring to a suspension of the crude 6 (10 g; 33.9 mmol) inwater (60 ml). The suspension was heated to 75° C. and kept at 75° C.for 2.5 hours to give a solution which was heated to 95° C. and kept at95° C. for 42 hours [ratio (2R,3R):(2R,3S)-thiomicamine=67:33]. Coolingthe solution to 15° C. caused the precipitation of a mixture of(-)-(1R,2R)-thiomicamine and compound as p-toluenesulphonates. After 1hour at 15° C. the salts were filtered and washed with water (20 ml);aqueous washings were combined together with mother liquors and saved(solution A). Sodium hydroxide (1.2 g; 30 mmol) was added at 25° C. to astirred suspension of the p-toluenesulphonates (12.1 g;(2R,3R):(2R,3S)-thiomicamine=76:24) in water (40 ml) up to pH 10.5. Thesolution was cooled to 5° C., the insoluble was filtered, washed withwater (20 ml) and dried under vacuum; aqueous washing were combined withthe mother liquors (solution B). The solid thiomicamine (4.3 g; HPLCassay 97%, (2R,3R):(2R,3S)-thiomicamine=96:4) was crystallized fromisopropanol (100 ml) at 5° C. to give analytically pure(2R,3R)-thiomicamine (3.4 g; yield 47%; [α]_(D) ²⁰ =-33.2° (c 2, 0.1NHCl); e.e.>99%).

Recycling of mother liquors: evaporation of the solvent from solution Bat 50° C. gave a residue (7.5 g; containing 1.74 g of (2R,3R) and(2R,3S)-thiomicamine in the ratio 84:16) which was suspended intopropan-2-ol (50 ml). The reaction mixture was heated to reflux andfiltered; the resulting solution was evaporated under reduced pressureto give a residue (2.3 g containing 1.64 g of (2R,3S) and(2R,3R)-thiomicamine in the ratio 84:16). The residue was combined withsolution A (85.2 g) and the solution was concentrated to 50 g undervacuum at 50° C. The mixture was heated under stirring at 90° C. for 24hours (ratio (2R,3S):(2R,3R)-thiomicamine=34:66; 2.36 g). The solutionwas cooled to 15° C. and the insoluble was filtered, dissolved at 25° C.under stirring in an aqueous solution of sodium hydroxide (0.3 g; 7.5mmol) in water (12 ml). The solution, having pH 10.5, was heated asabove to give crude thiomicamine (1.1 g; (2R,3R)-thiomicamine;d.e.>98.5%) which was crystallized from isopropanol to give pure(-)-(2R,3R)-thiomicamine (1.06 g; 15% yield; overall yield 62%)[α]_(D).sup. 20 =-33.8° (c 2, 0.1N HCl)

EXAMPLE 61

Acidic equilibration of (-)-(2R,3R)-thiomicamine

A solution of (2R,3R)-thiomicamine (10.0 g; 46.9 mmol) andp-toluenesulphonic acid monohydrated (20.0 g; 105.0 mmol) in water (60ml) was heated at 100° C. for 48 hours. HPLC analysis of the solutionshowed a ratio (2R,3R):(2R,3S)-thiomicamine=69:31, the total amountaccounting for 87% of the starting (2R,3R)-thiomicamine.

EXAMPLE 62

Preparation of(4R,5S)-5-(4-methylsulphonylphenyl)-3-acetyl-4-formyl-2,2-dimethyl-1,3-oxazolidine(Compound 39)

A mixture of compound 38 (1 g; 3 mmol), methylene chloride (7.5 ml),2,2,6,6-tetramethylpiperidinyl-1-oxy (TEMPO) (6.15 mg), potassiumbromide (40 mg) was cooled to 0° C. (water-ice bath). The mixture, undervigorous stirring, was added dropwise in 30 minutes to a solutionprepared by adding a 8% sodium bicarbonate aqueous solution (15 ml) andthen 1N HCl to sodium hypochlorite (3.7 ml; 7.8% w/v) (the pH of thesolution was 8.7). The mixture was stirred for 30 minutes at 0° C. andthe reaction was followed by TLC (silica gel, ethyl acetate as eluent).The phases were separated, the aqueous phase was extracted withmethylene chloride (3×10 ml), the combined organic extracts were washedwith a 5% sodium bicarbonate aqueous solution (10 ml) and with water (10ml). The organic phase was dried over sodium sulphate. Evaporation ofthe solvent under vacuum gave compound 39 (0.41 g) as residue.

EXAMPLE 63

Preparation of compound 6 from a mixture of compounds 4 and 5 (ratio5:4=50:50)

A mixture of compounds 5 and 4 (10 g; 34 mmol) (5:4=50:50) was added toa solution of citric acid (0.25 g) in ethanol (38 g). Sodium borohydride(0.15 g; 3.94 mmol) was added in two portion (the second after 15minutes) under stirring for 20 minutes and then was poured into a pH 7buffered aqueous solution (30 ml) and extracted with methylene chloride(30 ml). The combined organic extracts were washed with water and thesolvent was removed under vacuum to give a crude (10.7 g).

A mixture of 3 and 6 (2.04 g in the ratio 6:3=84:16) and a mixture of 4and 5 (6.7 g in the ratio 4:5=60:40) was obtained after usual work up.

EXAMPLE 64

Preparation of compound 4

p-Toluenesulphonylchloride (3.8 g; 0.02 mol) was added portionwise to acold mixture (0° C.) of compound 3 (2.95 g; 0.01 mol),dimethylsulphoxide (4.5 g; 0.058 mol) and toluene (7.5 ml).

The mixture was kept at 0° C. for 0.5 hours. Triethylamine (4 g; 0.04mol) was added dropwise at 0° C. and 5° C. under stirring in 1 hour tothe mixture. The reaction mixture was kept at 0° C. for 2 hours and thenpoured into water (20 ml). The organic phase was washed with 0.1Nhydrochloric acid (20 ml) and evaporated under vacuum to give a residue(2.8 g) containing compound 4 (2.3 g).

EXAMPLE 65

Preparation of compound 4

Benzenesulphonylchloride (3.5 g; 0.02 mol) was added portionwise to acold mixture (0° C.) of compound 3 (2.95 g; 0.01 mol),dimethylsulphoxide (6 g; 0.077 mol) and toluene (7.5 ml). The mixturewas kept at 0° C. for 0.5 hours. Triethylamine (4 g; 0.04 mol) was addeddropwise at 0° C. and 10° C. under stirring in 1 hour to the mixture.The reaction mixture was kept at 0° C. for 2 hours and then poured intowater (20 ml). The organic phase was washed with 0.1N hydrochloric acid(20 ml) and evaporated under vacuum to give a residue (2.7 g) containingcompound 4 (2.05 g).

EXAMPLE 66

Preparation of compound 4

2,4,6-Triisopropylbenzenesulphonylchloride (4.55 g; 0.015 mol) was addedportionwise to a cold mixture (-10° C.) of compound 3 (2.95 g; 0.01mol), dimethylsulphoxide (3.2 g; 0.04 mol) and methylene chloride (8ml).

The mixture was kept at -5° C. for 0.5 hours. Triethylamine (3 g; 0.03mol) was added dropwise at -5° C. and 0° C. under stirring in 30 minutesto the mixture. The reaction mixture was heated to 15° C. and kept at15° C. under stirring for 4 hours. The mixture was then poured intowater (20 ml). The organic phase was evaporated under vacuum to give aresidue (8 g) containing compound 4 (2 g).

EXAMPLE 67

Preparation of compound 4

2-Mesitylenesulphonylchloride (3.3 g; 0.015 mol) was added portion-wiseto a cold mixture (-10° C.) of compound 3 (2.95 g; 0.01 mol),dimethylsulphoxide (3.2 g; 0.04 mol) and methylene chloride (8 ml). Themixture was kept at -5° C. for 0.5 hours. Triethylamine (3 g; 0.03 mol)was added dropwise at -5° C. and 0° C. under stirring in 30 minutes tothe mixture. The reaction mixture was kept at 0° C. under stirring for 4hours. The mixture was then poured into water (20 ml). The organic phasewas evaporated under vacuum to give a residue (4.2 g) containingcompound 4 (2 g).

What we claim is:
 1. A compound of formula ##STR11## wherein R₂represents a lower alkyl, dichloromethyl, phenyl, alkoxy or benzyloxygroup;R₅ and R₆ together are the group C (R₃) (R₄)--wherein R₃ and R₄,equal to or different from each other, represent hydrogen atoms, loweralkyls, phenyls, lower alkoxy or R₃ and R₄ together are an oxygen atom,sulphur atom or a tetra or pentamethylene chain; and R₇ represents ahydrogen atom.
 2. The compound of claim 1 having the (2R,3S)configuration).
 3. The compound of claim 1 having the (2S,3S)configuration.